ClinVar Miner

List of variants reported as uncertain significance for brachydactyly type B1

Included ClinVar conditions (3):
Minimum submission review status: Collection method:
Minimum conflict level:
ClinVar version:
Total variants: 86
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HGVS dbSNP gnomAD frequency
NM_004560.4(ROR2):c.*553G>A rs769673512 0.00068
NM_004560.4(ROR2):c.*369G>C rs555728388 0.00048
NM_004560.4(ROR2):c.*135G>T rs774621355 0.00026
NM_004560.4(ROR2):c.-102G>T rs932588990 0.00022
NM_004560.4(ROR2):c.871A>G (p.Met291Val) rs150364724 0.00019
NM_004560.4(ROR2):c.-36A>G rs756061621 0.00014
NM_004560.4(ROR2):c.1601C>A (p.Pro534His) rs762554351 0.00013
NM_004560.4(ROR2):c.1885G>A (p.Val629Met) rs148844963 0.00011
NM_004560.4(ROR2):c.1940A>G (p.Lys647Arg) rs369059394 0.00011
NM_004560.4(ROR2):c.*38G>A rs367597436 0.00010
NM_004560.4(ROR2):c.1624G>A (p.Val542Met) rs140213020 0.00010
NM_004560.4(ROR2):c.1746G>A (p.Thr582=) rs201241207 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.1240A>G (p.Ile414Val) rs145023692 0.00007
NM_004560.4(ROR2):c.1105G>A (p.Gly369Arg) rs151187583 0.00006
NM_004560.4(ROR2):c.1997A>G (p.Tyr666Cys) rs1463489541 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.*433C>T rs919431237 0.00005
NM_004560.4(ROR2):c.*46C>T rs759105926 0.00005
NM_004560.4(ROR2):c.2521C>G (p.Gln841Glu) rs771461100 0.00005
NM_004560.4(ROR2):c.*487C>G rs970063320 0.00004
NM_004560.4(ROR2):c.*558C>T rs571058325 0.00004
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.281G>A (p.Arg94Gln) rs367829411 0.00004
NM_004560.4(ROR2):c.702C>T (p.Phe234=) rs559697443 0.00004
NM_004560.4(ROR2):c.864G>A (p.Ala288=) rs142926399 0.00004
NM_004560.4(ROR2):c.1552C>T (p.Arg518Trp) rs148896640 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.2080T>C (p.Cys694Arg) rs142386992 0.00003
NM_004560.4(ROR2):c.1154G>A (p.Arg385His) rs755135206 0.00002
NM_004560.4(ROR2):c.1399G>C (p.Glu467Gln) rs780576494 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.-154G>C rs1057515684 0.00001
NM_004560.4(ROR2):c.-66G>T rs1463989966 0.00001
NM_004560.4(ROR2):c.-90A>G rs1587871077 0.00001
NM_004560.4(ROR2):c.1279A>G (p.Met427Val) rs148390451 0.00001
NM_004560.4(ROR2):c.1300G>A (p.Ala434Thr) rs144447132 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.1566G>T (p.Arg522=) rs755724416 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.1820C>T (p.Ser607Phe) rs769849104 0.00001
NM_004560.4(ROR2):c.2155G>A (p.Ala719Thr) rs375448033 0.00001
NM_004560.4(ROR2):c.2458C>G (p.Pro820Ala) rs1253369894 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.768C>T (p.Cys256=) rs772113008 0.00001
NM_004560.4(ROR2):c.769G>A (p.Glu257Lys) rs543118807 0.00001
NM_004560.4(ROR2):c.904C>T (p.Arg302Cys) rs767372181 0.00001
NM_004560.4(ROR2):c.*107G>C rs189697737
NM_004560.4(ROR2):c.*125C>A rs1836869944
NM_004560.4(ROR2):c.*180C>A rs542396423
NM_004560.4(ROR2):c.*398G>C rs941756148
NM_004560.4(ROR2):c.*571G>C rs1836854224
NM_004560.4(ROR2):c.*682C>G rs1057515678
NM_004560.4(ROR2):c.-118C>T rs1832134851
NM_004560.4(ROR2):c.-135G>C rs1057515683
NM_004560.4(ROR2):c.1103C>G (p.Pro368Arg) rs1716064320
NM_004560.4(ROR2):c.1234A>G (p.Ile412Val) rs1057515681
NM_004560.4(ROR2):c.1347C>G (p.Ser449Arg) rs1837043278
NM_004560.4(ROR2):c.1412C>T (p.Ser471Phe) rs1564230209
NM_004560.4(ROR2):c.1510G>A (p.Val504Met) rs2118626430
NM_004560.4(ROR2):c.1644C>A (p.Pro548=) rs1836960066
NM_004560.4(ROR2):c.179A>C (p.Tyr60Ser) rs768160554
NM_004560.4(ROR2):c.1870T>A (p.Tyr624Asn) rs1836942190
NM_004560.4(ROR2):c.2014G>A (p.Asp672Asn) rs55651110
NM_004560.4(ROR2):c.2208G>T (p.Arg736=) rs1587653081
NM_004560.4(ROR2):c.2242G>T (p.Ala748Ser) rs1836916256
NM_004560.4(ROR2):c.2314T>A (p.Ser772Thr) rs1057515680
NM_004560.4(ROR2):c.2782G>A (p.Asp928Asn) rs199855010
NM_004560.4(ROR2):c.731G>A (p.Arg244Gln) rs55737262
NM_004560.4(ROR2):c.886G>A (p.Asp296Asn) rs867038828
NM_004560.4(ROR2):c.938-15G>A rs1837231210
NM_004560.4(ROR2):c.989C>T (p.Thr330Ile) rs1837228232

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