ClinVar Miner

List of variants in gene ROR2 reported as uncertain significance for not provided

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 253
Download table as spreadsheet
HGVS dbSNP gnomAD frequency
NM_004560.4(ROR2):c.2285C>T (p.Ser762Leu) rs34491822 0.00357
NM_004560.4(ROR2):c.2395C>T (p.Pro799Ser) rs141235720 0.00173
NM_004560.4(ROR2):c.1583G>A (p.Arg528Gln) rs142215888 0.00108
NM_004560.4(ROR2):c.1670C>T (p.Ser557Leu) rs56099091 0.00098
NM_004560.4(ROR2):c.1736A>T (p.Asp579Val) rs150610444 0.00092
NM_004560.4(ROR2):c.2461G>A (p.Val821Ile) rs149056068 0.00086
NM_004560.4(ROR2):c.234G>A (p.Thr78=) rs141093530 0.00046
NM_004560.4(ROR2):c.2684A>G (p.Asp895Gly) rs149826387 0.00038
NM_004560.4(ROR2):c.1671G>A (p.Ser557=) rs201232887 0.00024
NM_004560.4(ROR2):c.1675G>A (p.Gly559Ser) rs117134265 0.00019
NM_004560.4(ROR2):c.568A>G (p.Thr190Ala) rs34574788 0.00019
NM_004560.4(ROR2):c.871A>G (p.Met291Val) rs150364724 0.00019
NM_004560.4(ROR2):c.2698G>A (p.Ala900Thr) rs202213533 0.00017
NM_004560.4(ROR2):c.380C>T (p.Thr127Met) rs375080866 0.00017
NM_004560.4(ROR2):c.808A>G (p.Ile270Val) rs145631389 0.00017
NM_004560.4(ROR2):c.1601C>A (p.Pro534His) rs762554351 0.00013
NM_004560.4(ROR2):c.1940A>G (p.Lys647Arg) rs369059394 0.00013
NM_004560.4(ROR2):c.2286G>A (p.Ser762=) rs143759440 0.00012
NM_004560.4(ROR2):c.1885G>A (p.Val629Met) rs148844963 0.00011
NM_004560.4(ROR2):c.1606G>A (p.Val536Ile) rs145088924 0.00010
NM_004560.4(ROR2):c.1624G>A (p.Val542Met) rs140213020 0.00010
NM_004560.4(ROR2):c.2240G>A (p.Arg747Gln) rs201155263 0.00010
NM_004560.4(ROR2):c.2782G>C (p.Asp928His) rs199855010 0.00009
NM_004560.4(ROR2):c.1490C>T (p.Pro497Leu) rs772631240 0.00008
NM_004560.4(ROR2):c.1565G>A (p.Arg522Gln) rs201986784 0.00008
NM_004560.4(ROR2):c.2143G>A (p.Asp715Asn) rs201994918 0.00008
NM_004560.4(ROR2):c.1240A>G (p.Ile414Val) rs145023692 0.00007
NM_004560.4(ROR2):c.1448G>A (p.Arg483Gln) rs767474960 0.00007
NM_004560.4(ROR2):c.233C>T (p.Thr78Met) rs369545969 0.00007
NM_004560.4(ROR2):c.2628G>A (p.Thr876=) rs369201767 0.00007
NM_004560.4(ROR2):c.1105G>A (p.Gly369Arg) rs151187583 0.00006
NM_004560.4(ROR2):c.1756G>A (p.Ala586Thr) rs142386294 0.00006
NM_004560.4(ROR2):c.1997A>G (p.Tyr666Cys) rs1463489541 0.00006
NM_004560.4(ROR2):c.2445G>A (p.Pro815=) rs202010959 0.00006
NM_004560.4(ROR2):c.37C>G (p.Leu13Val) rs1053014086 0.00006
NM_004560.4(ROR2):c.678C>T (p.Phe226=) rs202159869 0.00006
NM_004560.4(ROR2):c.1927G>A (p.Ala643Thr) rs771184180 0.00005
NM_004560.4(ROR2):c.2521C>G (p.Gln841Glu) rs771461100 0.00005
NM_004560.4(ROR2):c.822C>T (p.Asn274=) rs140557090 0.00005
NM_004560.4(ROR2):c.863C>T (p.Ala288Val) rs138087167 0.00005
NM_004560.4(ROR2):c.1553G>A (p.Arg518Gln) rs373544528 0.00004
NM_004560.4(ROR2):c.1630A>G (p.Thr544Ala) rs374811924 0.00004
NM_004560.4(ROR2):c.1732G>A (p.Asp578Asn) rs139802697 0.00004
NM_004560.4(ROR2):c.175+3G>T rs557936422 0.00004
NM_004560.4(ROR2):c.1913G>A (p.Arg638Gln) rs765278167 0.00004
NM_004560.4(ROR2):c.2424C>T (p.Ile808=) rs376416766 0.00004
NM_004560.4(ROR2):c.2649G>A (p.Met883Ile) rs373037095 0.00004
NM_004560.4(ROR2):c.281G>A (p.Arg94Gln) rs367829411 0.00004
NM_004560.4(ROR2):c.934C>T (p.Arg312Cys) rs776683439 0.00004
NM_004560.4(ROR2):c.1285C>T (p.Arg429Trp) rs772321377 0.00003
NM_004560.4(ROR2):c.1564C>T (p.Arg522Trp) rs748786708 0.00003
NM_004560.4(ROR2):c.1574C>G (p.Ala525Gly) rs34584753 0.00003
NM_004560.4(ROR2):c.1799C>T (p.Ala600Val) rs143738026 0.00003
NM_004560.4(ROR2):c.1873G>A (p.Asp625Asn) rs754476697 0.00003
NM_004560.4(ROR2):c.1966A>G (p.Ile656Val) rs1239750233 0.00003
NM_004560.4(ROR2):c.2080T>C (p.Cys694Arg) rs142386992 0.00003
NM_004560.4(ROR2):c.51C>A (p.Ala17=) rs886043361 0.00003
NM_004560.4(ROR2):c.1154G>A (p.Arg385His) rs755135206 0.00002
NM_004560.4(ROR2):c.1236C>T (p.Ile412=) rs752218712 0.00002
NM_004560.4(ROR2):c.1321C>T (p.Arg441Trp) rs762451478 0.00002
NM_004560.4(ROR2):c.1360A>G (p.Met454Val) rs771198485 0.00002
NM_004560.4(ROR2):c.1399G>C (p.Glu467Gln) rs780576494 0.00002
NM_004560.4(ROR2):c.1604A>G (p.Asn535Ser) rs772789770 0.00002
NM_004560.4(ROR2):c.1678G>A (p.Asp560Asn) rs148793424 0.00002
NM_004560.4(ROR2):c.1771G>A (p.Asp591Asn) rs768175141 0.00002
NM_004560.4(ROR2):c.2206C>T (p.Arg736Trp) rs1329621652 0.00002
NM_004560.4(ROR2):c.2354G>A (p.Arg785His) rs368059807 0.00002
NM_004560.4(ROR2):c.496G>T (p.Asp166Tyr) rs767615145 0.00002
NM_004560.4(ROR2):c.663C>G (p.Asp221Glu) rs1461699343 0.00002
NM_004560.4(ROR2):c.1054A>G (p.Ser352Gly) rs569242465 0.00001
NM_004560.4(ROR2):c.1153C>T (p.Arg385Cys) rs777538346 0.00001
NM_004560.4(ROR2):c.1255G>A (p.Ala419Thr) rs762871988 0.00001
NM_004560.4(ROR2):c.1279A>G (p.Met427Val) rs148390451 0.00001
NM_004560.4(ROR2):c.1322G>A (p.Arg441Gln) rs142993413 0.00001
NM_004560.4(ROR2):c.1502C>A (p.Thr501Asn) rs142047260 0.00001
NM_004560.4(ROR2):c.1639C>A (p.Gln547Lys) rs1489863862 0.00001
NM_004560.4(ROR2):c.1687G>A (p.Glu563Lys) rs186571882 0.00001
NM_004560.4(ROR2):c.1715C>T (p.Ser572Leu) rs1468411890 0.00001
NM_004560.4(ROR2):c.1757C>T (p.Ala586Val) rs763556461 0.00001
NM_004560.4(ROR2):c.1820C>T (p.Ser607Phe) rs769849104 0.00001
NM_004560.4(ROR2):c.1955C>T (p.Ser652Leu) rs541919750 0.00001
NM_004560.4(ROR2):c.2155G>A (p.Ala719Thr) rs375448033 0.00001
NM_004560.4(ROR2):c.2203C>T (p.Arg735Trp) rs761169064 0.00001
NM_004560.4(ROR2):c.2239C>T (p.Arg747Ter) rs374646337 0.00001
NM_004560.4(ROR2):c.2359G>A (p.Val787Met) rs1219060338 0.00001
NM_004560.4(ROR2):c.2489A>G (p.Tyr830Cys) rs775640546 0.00001
NM_004560.4(ROR2):c.2550G>C (p.Gln850His) rs1424299048 0.00001
NM_004560.4(ROR2):c.2725G>C (p.Val909Leu) rs778811682 0.00001
NM_004560.4(ROR2):c.2770G>C (p.Glu924Gln) rs766605383 0.00001
NM_004560.4(ROR2):c.2828C>A (p.Ala943Asp) rs199840505 0.00001
NM_004560.4(ROR2):c.302C>T (p.Pro101Leu) rs370882834 0.00001
NM_004560.4(ROR2):c.334C>T (p.Arg112Trp) rs868585233 0.00001
NM_004560.4(ROR2):c.457C>T (p.Arg153Trp) rs745695427 0.00001
NM_004560.4(ROR2):c.533G>A (p.Arg178Gln) rs746562213 0.00001
NM_004560.4(ROR2):c.622G>A (p.Ala208Thr) rs1825065690 0.00001
NM_004560.4(ROR2):c.626C>T (p.Ala209Val) rs768469342 0.00001
NM_004560.4(ROR2):c.746G>A (p.Arg249His) rs1347793502 0.00001
NM_004560.4(ROR2):c.769G>A (p.Glu257Lys) rs543118807 0.00001
NM_004560.4(ROR2):c.922G>A (p.Glu308Lys) rs761854477 0.00001
NM_004560.4(ROR2):c.938-6G>C rs769467387 0.00001
NC_000009.11:g.(?_94712129)_(94712245_?)dup
NM_004560.4(ROR2):c.1016C>T (p.Pro339Leu)
NM_004560.4(ROR2):c.1034C>G (p.Pro345Arg)
NM_004560.4(ROR2):c.1079G>C (p.Gly360Ala)
NM_004560.4(ROR2):c.1117G>A (p.Glu373Lys)
NM_004560.4(ROR2):c.1148A>G (p.Asn383Ser)
NM_004560.4(ROR2):c.1165T>C (p.Cys389Arg)
NM_004560.4(ROR2):c.1174C>T (p.Pro392Ser)
NM_004560.4(ROR2):c.1199G>C (p.Ser400Thr)
NM_004560.4(ROR2):c.119C>T (p.Pro40Leu)
NM_004560.4(ROR2):c.1251C>T (p.Val417=) rs794727918
NM_004560.4(ROR2):c.1272G>A (p.Leu424=)
NM_004560.4(ROR2):c.1286G>A (p.Arg429Gln)
NM_004560.4(ROR2):c.1300G>C (p.Ala434Pro)
NM_004560.4(ROR2):c.1316C>T (p.Pro439Leu)
NM_004560.4(ROR2):c.1325G>A (p.Arg442Gln)
NM_004560.4(ROR2):c.1331T>G (p.Leu444Arg)
NM_004560.4(ROR2):c.1339T>G (p.Ser447Ala) rs794727917
NM_004560.4(ROR2):c.1340C>T (p.Ser447Leu)
NM_004560.4(ROR2):c.1355T>C (p.Met452Thr)
NM_004560.4(ROR2):c.1366C>T (p.Leu456Phe)
NM_004560.4(ROR2):c.1369A>G (p.Ile457Val)
NM_004560.4(ROR2):c.137C>A (p.Pro46His)
NM_004560.4(ROR2):c.1400A>G (p.Glu467Gly) rs1564230248
NM_004560.4(ROR2):c.140T>A (p.Leu47His)
NM_004560.4(ROR2):c.1412C>T (p.Ser471Phe) rs1564230209
NM_004560.4(ROR2):c.1422G>T (p.Arg474Ser)
NM_004560.4(ROR2):c.1436T>C (p.Leu479Pro)
NM_004560.4(ROR2):c.145G>T (p.Gly49Trp)
NM_004560.4(ROR2):c.1490C>A (p.Pro497Gln)
NM_004560.4(ROR2):c.1495G>C (p.Glu499Gln)
NM_004560.4(ROR2):c.1531G>A (p.Asp511Asn)
NM_004560.4(ROR2):c.1538C>T (p.Ala513Val)
NM_004560.4(ROR2):c.154G>A (p.Gly52Ser)
NM_004560.4(ROR2):c.1576A>G (p.Met526Val)
NM_004560.4(ROR2):c.1603_1605del (p.Asn535del)
NM_004560.4(ROR2):c.1639_1677dup (p.Gln547_Gly559dup) rs2118622964
NM_004560.4(ROR2):c.1646T>C (p.Leu549Pro)
NM_004560.4(ROR2):c.1706C>T (p.Ser569Leu)
NM_004560.4(ROR2):c.1720G>A (p.Val574Met)
NM_004560.4(ROR2):c.1736A>G (p.Asp579Gly) rs150610444
NM_004560.4(ROR2):c.1739A>T (p.Asp580Val)
NM_004560.4(ROR2):c.1742G>A (p.Arg581His)
NM_004560.4(ROR2):c.1745C>T (p.Thr582Met)
NM_004560.4(ROR2):c.174A>G (p.Lys58=) rs886042213
NM_004560.4(ROR2):c.175+5G>A
NM_004560.4(ROR2):c.1777G>A (p.Val593Met)
NM_004560.4(ROR2):c.1794G>C (p.Gln598His)
NM_004560.4(ROR2):c.1802C>G (p.Ala601Gly)
NM_004560.4(ROR2):c.1807A>G (p.Met603Val)
NM_004560.4(ROR2):c.1811A>G (p.Glu604Gly)
NM_004560.4(ROR2):c.1823G>A (p.Ser608Asn)
NM_004560.4(ROR2):c.1831G>A (p.Val611Met)
NM_004560.4(ROR2):c.1841A>G (p.Lys614Arg)
NM_004560.4(ROR2):c.1852A>G (p.Thr618Ala)
NM_004560.4(ROR2):c.1853C>T (p.Thr618Ile)
NM_004560.4(ROR2):c.2014G>A (p.Asp672Asn) rs55651110
NM_004560.4(ROR2):c.2014G>T (p.Asp672Tyr) rs55651110
NM_004560.4(ROR2):c.2030C>T (p.Ser677Phe) rs2118617134
NM_004560.4(ROR2):c.2062T>G (p.Tyr688Asp)
NM_004560.4(ROR2):c.2107G>A (p.Glu703Lys)
NM_004560.4(ROR2):c.2116C>T (p.Arg706Trp)
NM_004560.4(ROR2):c.2134C>T (p.Pro712Ser)
NM_004560.4(ROR2):c.2135C>T (p.Pro712Leu)
NM_004560.4(ROR2):c.2150G>C (p.Cys717Ser)
NM_004560.4(ROR2):c.2191G>A (p.Glu731Lys)
NM_004560.4(ROR2):c.219T>G (p.Ile73Met)
NM_004560.4(ROR2):c.2204G>A (p.Arg735Gln)
NM_004560.4(ROR2):c.2213G>A (p.Arg738His)
NM_004560.4(ROR2):c.2230A>T (p.Ser744Cys)
NM_004560.4(ROR2):c.2233C>T (p.Arg745Trp) rs749323904
NM_004560.4(ROR2):c.2236C>T (p.Leu746Phe) rs1836916811
NM_004560.4(ROR2):c.2249G>A (p.Gly750Asp) rs552528721
NM_004560.4(ROR2):c.2267A>G (p.Asn756Ser) rs2118612912
NM_004560.4(ROR2):c.2273C>T (p.Ser758Leu)
NM_004560.4(ROR2):c.2290del (p.Ala764fs)
NM_004560.4(ROR2):c.2305C>T (p.Gln769Ter) rs1836911147
NM_004560.4(ROR2):c.231G>C (p.Gln77His)
NM_004560.4(ROR2):c.2320A>C (p.Ser774Arg)
NM_004560.4(ROR2):c.233C>G (p.Thr78Arg) rs369545969
NM_004560.4(ROR2):c.2350G>A (p.Ala784Thr)
NM_004560.4(ROR2):c.2374A>G (p.Lys792Glu)
NM_004560.4(ROR2):c.2378C>T (p.Ala793Val) rs774317100
NM_004560.4(ROR2):c.2411T>C (p.Met804Thr)
NM_004560.4(ROR2):c.2415G>A (p.Lys805=) rs2118610452
NM_004560.4(ROR2):c.2428C>A (p.Pro810Thr)
NM_004560.4(ROR2):c.2443_2517del (p.Pro815_Pro839del) rs2118608399
NM_004560.4(ROR2):c.2446C>A (p.Gln816Lys)
NM_004560.4(ROR2):c.2467G>A (p.Gly823Ser) rs753371692
NM_004560.4(ROR2):c.2477C>A (p.Pro826Gln)
NM_004560.4(ROR2):c.2479G>T (p.Val827Leu)
NM_004560.4(ROR2):c.2485G>A (p.Ala829Thr)
NM_004560.4(ROR2):c.2517G>C (p.Pro839=) rs373575567
NM_004560.4(ROR2):c.2523G>C (p.Gln841His) rs1280968883
NM_004560.4(ROR2):c.2549A>T (p.Gln850Leu)
NM_004560.4(ROR2):c.2555CTC[1] (p.Pro853del) rs772604181
NM_004560.4(ROR2):c.256G>T (p.Ala86Ser) rs747477231
NM_004560.4(ROR2):c.2582C>T (p.Ser861Leu) rs1564226947
NM_004560.4(ROR2):c.2597G>C (p.Ser866Thr)
NM_004560.4(ROR2):c.25C>G (p.Arg9Gly) rs1832129314
NM_004560.4(ROR2):c.2627C>T (p.Thr876Met)
NM_004560.4(ROR2):c.2633C>A (p.Pro878His)
NM_004560.4(ROR2):c.2645C>G (p.Ser882Cys)
NM_004560.4(ROR2):c.2693A>G (p.Gln898Arg)
NM_004560.4(ROR2):c.2713G>C (p.Ala905Pro) rs779855786
NM_004560.4(ROR2):c.2725G>A (p.Val909Met) rs778811682
NM_004560.4(ROR2):c.2731G>A (p.Glu911Lys)
NM_004560.4(ROR2):c.2747A>C (p.Glu916Ala)
NM_004560.4(ROR2):c.277G>A (p.Val93Met)
NM_004560.4(ROR2):c.2789A>T (p.Asp930Val)
NM_004560.4(ROR2):c.2794_2795del (p.Leu932fs)
NM_004560.4(ROR2):c.280C>T (p.Arg94Trp)
NM_004560.4(ROR2):c.2820G>C (p.Gln940His) rs113793278
NM_004560.4(ROR2):c.298G>A (p.Ala100Thr) rs374692105
NM_004560.4(ROR2):c.329T>C (p.Ile110Thr) rs1825791727
NM_004560.4(ROR2):c.377A>C (p.Asp126Ala)
NM_004560.4(ROR2):c.378C>A (p.Asp126Glu)
NM_004560.4(ROR2):c.388A>T (p.Thr130Ser)
NM_004560.4(ROR2):c.394T>C (p.Tyr132His)
NM_004560.4(ROR2):c.406G>A (p.Val136Met)
NM_004560.4(ROR2):c.448C>G (p.Leu150Val)
NM_004560.4(ROR2):c.536G>T (p.Gly179Val) rs1825071241
NM_004560.4(ROR2):c.604A>G (p.Ile202Val)
NM_004560.4(ROR2):c.623-11G>A rs1350375399
NM_004560.4(ROR2):c.623C>T (p.Ala208Val)
NM_004560.4(ROR2):c.634A>G (p.Met212Val) rs2118703110
NM_004560.4(ROR2):c.637A>G (p.Ile213Val)
NM_004560.4(ROR2):c.640G>A (p.Gly214Ser)
NM_004560.4(ROR2):c.703G>A (p.Val235Met) rs140179632
NM_004560.4(ROR2):c.722C>A (p.Ala241Glu) rs771096772
NM_004560.4(ROR2):c.722C>T (p.Ala241Val)
NM_004560.4(ROR2):c.725G>A (p.Arg242His) rs756285939
NM_004560.4(ROR2):c.731G>C (p.Arg244Pro)
NM_004560.4(ROR2):c.743C>T (p.Pro248Leu)
NM_004560.4(ROR2):c.752T>C (p.Leu251Pro)
NM_004560.4(ROR2):c.757C>T (p.Arg253Cys)
NM_004560.4(ROR2):c.765G>C (p.Glu255Asp) rs1223420477
NM_004560.4(ROR2):c.769_770delinsTT (p.Glu257Leu) rs2118701033
NM_004560.4(ROR2):c.794G>A (p.Arg265His)
NM_004560.4(ROR2):c.824C>T (p.Pro275Leu)
NM_004560.4(ROR2):c.82G>A (p.Val28Met)
NM_004560.4(ROR2):c.835A>G (p.Met279Val)
NM_004560.4(ROR2):c.853A>G (p.Lys285Glu)
NM_004560.4(ROR2):c.879G>C (p.Glu293Asp) rs1445408805
NM_004560.4(ROR2):c.886G>A (p.Asp296Asn) rs867038828
NM_004560.4(ROR2):c.888C>G (p.Asp296Glu)
NM_004560.4(ROR2):c.88C>G (p.Arg30Gly)
NM_004560.4(ROR2):c.902T>A (p.Met301Lys) rs2118699388
NM_004560.4(ROR2):c.902T>C (p.Met301Thr)
NM_004560.4(ROR2):c.929T>G (p.Leu310Arg) rs2118698909
NM_004560.4(ROR2):c.934C>A (p.Arg312Ser)
NM_004560.4(ROR2):c.941A>G (p.His314Arg)
NM_004560.4(ROR2):c.980C>T (p.Thr327Met)

The information on this website is not intended for direct diagnostic use or medical decision-making without review by a genetics professional. Individuals should not change their health behavior solely on the basis of information contained on this website. Neither the University of Utah nor the National Institutes of Health independently verfies the submitted information. If you have questions about the information contained on this website, please see a health care professional.