ClinVar Miner

List of variants reported as uncertain significance for Brachydactyly type B1; Autosomal recessive Robinow syndrome by Fulgent Genetics, Fulgent Genetics

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Total variants: 44
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HGVS dbSNP gnomAD frequency
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.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.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.2521C>G (p.Gln841Glu) rs771461100 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.281G>A (p.Arg94Gln) rs367829411 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.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.2155G>A (p.Ala719Thr) rs375448033 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.1412C>T (p.Ser471Phe) rs1564230209
NM_004560.4(ROR2):c.2014G>A (p.Asp672Asn) rs55651110

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