ClinVar Miner

List of variants in gene ROR2 reported by Eurofins NTD LLC (GA)

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Gene type:
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Total variants: 64
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HGVS dbSNP gnomAD frequency
NM_004560.4(ROR2):c.*16G>A rs2230578 0.73170
NM_004560.4(ROR2):c.2455G>A (p.Val819Ile) rs10761129 0.71630
NM_004560.4(ROR2):c.733A>G (p.Thr245Ala) rs10820900 0.66416
NM_004560.4(ROR2):c.2088C>T (p.Tyr696=) rs10992063 0.44353
NM_004560.4(ROR2):c.2154C>T (p.Pro718=) rs2230577 0.05836
NM_004560.4(ROR2):c.75G>A (p.Leu25=) rs148237260 0.01389
NM_004560.4(ROR2):c.2727G>A (p.Val909=) rs56091954 0.01249
NM_004560.4(ROR2):c.2285C>T (p.Ser762Leu) rs34491822 0.00357
NM_004560.4(ROR2):c.937+10C>T rs201083970 0.00310
NM_004560.4(ROR2):c.7C>T (p.Arg3Trp) rs539329891 0.00261
NM_004560.4(ROR2):c.372C>T (p.Asp124=) rs145568368 0.00241
NM_004560.4(ROR2):c.1686C>T (p.His562=) rs56048121 0.00232
NM_004560.4(ROR2):c.2083G>A (p.Gly695Arg) rs34431454 0.00174
NM_004560.4(ROR2):c.2395C>T (p.Pro799Ser) rs141235720 0.00173
NM_004560.4(ROR2):c.1589G>A (p.Arg530Gln) rs35852786 0.00156
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.730C>T (p.Arg244Trp) rs148340413 0.00035
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.380C>T (p.Thr127Met) rs375080866 0.00017
NM_004560.4(ROR2):c.808A>G (p.Ile270Val) rs145631389 0.00017
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.2466C>T (p.Asn822=) rs146432734 0.00011
NM_004560.4(ROR2):c.2240G>A (p.Arg747Gln) rs201155263 0.00010
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.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.1756G>A (p.Ala586Thr) rs142386294 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.1712A>G (p.His571Arg) rs376970201 0.00005
NM_004560.4(ROR2):c.822C>T (p.Asn274=) rs140557090 0.00005
NM_004560.4(ROR2):c.2424C>T (p.Ile808=) rs376416766 0.00004
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.1236C>T (p.Ile412=) rs752218712 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.2155G>A (p.Ala719Thr) rs375448033 0.00001
NM_004560.4(ROR2):c.2489A>G (p.Tyr830Cys) rs775640546 0.00001
NM_004560.4(ROR2):c.938-6G>C rs769467387 0.00001
NM_004560.4(ROR2):c.1251C>T (p.Val417=) rs794727918
NM_004560.4(ROR2):c.1339T>G (p.Ser447Ala) rs794727917
NM_004560.4(ROR2):c.1736A>G (p.Asp579Gly) rs150610444
NM_004560.4(ROR2):c.174A>G (p.Lys58=) rs886042213
NM_004560.4(ROR2):c.2130_2151dup (p.Pro718delinsAlaAlaLeuProArgTer) rs886042428
NM_004560.4(ROR2):c.233C>G (p.Thr78Arg) rs369545969
NM_004560.4(ROR2):c.2517G>C (p.Pro839=) rs373575567
NM_004560.4(ROR2):c.2582C>T (p.Ser861Leu) rs1564226947
NM_004560.4(ROR2):c.2805C>G (p.Asp935Glu) rs41277835
NM_004560.4(ROR2):c.298G>A (p.Ala100Thr) rs374692105

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