ClinVar Miner

List of variants in gene INF2 reported as uncertain significance by GeneDx

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Gene type:
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Total variants: 18
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HGVS dbSNP
NM_022489.4(INF2):c.1+1G>C rs758452999
NM_022489.4(INF2):c.1147G>A (p.Val383Met) rs780689756
NM_022489.4(INF2):c.1183G>A (p.Glu395Lys) rs374769850
NM_022489.4(INF2):c.1189G>A (p.Val397Met) rs771775245
NM_022489.4(INF2):c.1288C>T (p.Leu430Phe) rs1131691501
NM_022489.4(INF2):c.1360C>T (p.Leu454Phe) rs545495465
NM_022489.4(INF2):c.1589del (p.Val530fs) rs879254321
NM_022489.4(INF2):c.1666C>T (p.Arg556Trp) rs879254313
NM_022489.4(INF2):c.2005G>A (p.Val669Met) rs756038490
NM_022489.4(INF2):c.2726C>A (p.Thr909Lys) rs201336550
NM_022489.4(INF2):c.2875C>T (p.Pro959Ser) rs369417066
NM_022489.4(INF2):c.2879-20G>C rs879254306
NM_022489.4(INF2):c.2897A>G (p.Lys966Arg) rs879254296
NM_022489.4(INF2):c.3356A>C (p.Asn1119Thr) rs200246759
NM_022489.4(INF2):c.3494C>T (p.Ala1165Val) rs771044828
NM_022489.4(INF2):c.3535A>G (p.Thr1179Ala) rs778879482
NM_022489.4(INF2):c.3583G>C (p.Glu1195Gln) rs1064796974
NM_022489.4(INF2):c.67T>A (p.Ser23Thr) rs746964937

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