ClinVar Miner

List of variants in gene ADGRG2 reported as uncertain significance for Inborn genetic diseases

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Total variants: 57
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HGVS dbSNP gnomAD frequency
NM_001079858.3(ADGRG2):c.2675G>A (p.Arg892Gln) rs142899178 0.00141
NM_001079858.3(ADGRG2):c.26G>A (p.Gly9Asp) rs73445689 0.00089
NM_001079858.3(ADGRG2):c.533C>A (p.Thr178Lys) rs201435414 0.00071
NM_001079858.3(ADGRG2):c.2359T>C (p.Tyr787His) rs141079424 0.00030
NM_001079858.3(ADGRG2):c.1010C>T (p.Thr337Ile) rs201217715 0.00018
NM_001079858.3(ADGRG2):c.2008G>A (p.Ala670Thr) rs186496373 0.00016
NM_001079858.3(ADGRG2):c.551C>T (p.Thr184Ile) rs778170129 0.00013
NM_001079858.3(ADGRG2):c.973A>G (p.Ile325Val) rs750786969 0.00008
NM_001079858.3(ADGRG2):c.1538A>G (p.Asn513Ser) rs143528070 0.00007
NM_001079858.3(ADGRG2):c.2729C>T (p.Thr910Ile) rs377045888 0.00006
NM_001079858.3(ADGRG2):c.1100A>C (p.Asp367Ala) rs370533807 0.00003
NM_001079858.3(ADGRG2):c.1682C>T (p.Pro561Leu) rs760652148 0.00003
NM_001079858.3(ADGRG2):c.1778A>G (p.Asp593Gly) rs755136941 0.00002
NM_001079858.3(ADGRG2):c.2360A>G (p.Tyr787Cys) rs757924540 0.00002
NM_001079858.3(ADGRG2):c.2698C>T (p.Arg900Trp) rs746674412 0.00002
NM_001079858.3(ADGRG2):c.965C>T (p.Ser322Phe) rs747325462 0.00002
NM_001079858.3(ADGRG2):c.1481C>T (p.Ser494Leu) rs754391347 0.00001
NM_001079858.3(ADGRG2):c.1631C>T (p.Thr544Ile) rs367571716 0.00001
NM_001079858.3(ADGRG2):c.2456A>C (p.Lys819Thr) rs1319398484 0.00001
NM_001079858.3(ADGRG2):c.2857G>A (p.Ala953Thr) rs745533304 0.00001
NM_001079858.3(ADGRG2):c.1040C>T (p.Ser347Phe)
NM_001079858.3(ADGRG2):c.1064A>T (p.Asn355Ile)
NM_001079858.3(ADGRG2):c.1180G>C (p.Glu394Gln)
NM_001079858.3(ADGRG2):c.1200A>C (p.Glu400Asp)
NM_001079858.3(ADGRG2):c.1367A>G (p.Asn456Ser)
NM_001079858.3(ADGRG2):c.1465A>G (p.Ile489Val)
NM_001079858.3(ADGRG2):c.1504C>T (p.His502Tyr)
NM_001079858.3(ADGRG2):c.1571C>T (p.Pro524Leu)
NM_001079858.3(ADGRG2):c.1828G>A (p.Gly610Ser)
NM_001079858.3(ADGRG2):c.2063A>T (p.Tyr688Phe)
NM_001079858.3(ADGRG2):c.2123C>T (p.Ser708Leu)
NM_001079858.3(ADGRG2):c.2299G>A (p.Gly767Arg)
NM_001079858.3(ADGRG2):c.2305T>A (p.Phe769Ile) rs2518667104
NM_001079858.3(ADGRG2):c.2417T>C (p.Ile806Thr)
NM_001079858.3(ADGRG2):c.2455A>C (p.Lys819Gln)
NM_001079858.3(ADGRG2):c.2482A>G (p.Ser828Gly)
NM_001079858.3(ADGRG2):c.2485A>G (p.Ile829Val)
NM_001079858.3(ADGRG2):c.2583G>A (p.Met861Ile)
NM_001079858.3(ADGRG2):c.2704G>A (p.Ala902Thr) rs1243499570
NM_001079858.3(ADGRG2):c.2726A>G (p.Lys909Arg)
NM_001079858.3(ADGRG2):c.2956A>G (p.Met986Val)
NM_001079858.3(ADGRG2):c.2996G>A (p.Arg999His)
NM_001079858.3(ADGRG2):c.3035A>G (p.His1012Arg) rs2518624644
NM_001079858.3(ADGRG2):c.307G>A (p.Val103Ile)
NM_001079858.3(ADGRG2):c.332A>G (p.Asn111Ser) rs2518839697
NM_001079858.3(ADGRG2):c.428C>T (p.Thr143Met)
NM_001079858.3(ADGRG2):c.443C>T (p.Thr148Ile)
NM_001079858.3(ADGRG2):c.522A>G (p.Ile174Met)
NM_001079858.3(ADGRG2):c.646C>T (p.His216Tyr) rs2518775831
NM_001079858.3(ADGRG2):c.66G>T (p.Lys22Asn) rs745874668
NM_001079858.3(ADGRG2):c.695T>C (p.Leu232Ser)
NM_001079858.3(ADGRG2):c.794C>T (p.Pro265Leu)
NM_001079858.3(ADGRG2):c.797G>C (p.Arg266Pro) rs750514534
NM_001079858.3(ADGRG2):c.812C>T (p.Ser271Phe)
NM_001079858.3(ADGRG2):c.881C>T (p.Ser294Phe)
NM_001079858.3(ADGRG2):c.890G>T (p.Gly297Val)
NM_001079858.3(ADGRG2):c.916C>G (p.Pro306Ala)

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