ClinVar Miner

List of variants reported as uncertain significance for type 2 diabetes mellitus by Labcorp Genetics (formerly Invitae), Labcorp

Included ClinVar conditions (37):
Minimum submission review status: Collection method:
Minimum conflict level:
ClinVar version:
Total variants: 43
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HGVS dbSNP gnomAD frequency
NM_001626.6(AKT2):c.347G>C (p.Gly116Ala) rs141209878 0.00036
NM_001626.6(AKT2):c.623G>A (p.Arg208Lys) rs35817154 0.00029
NM_001626.6(AKT2):c.1399C>T (p.Arg467Trp) rs142926499 0.00019
NM_001626.6(AKT2):c.1115C>T (p.Thr372Met) rs139506765 0.00011
NM_001626.6(AKT2):c.395C>T (p.Thr132Met) rs143335817 0.00005
NM_001626.6(AKT2):c.19A>G (p.Ile7Val) rs199748431 0.00004
NM_001626.6(AKT2):c.1112G>A (p.Arg371His) rs778561687 0.00003
NM_001626.6(AKT2):c.526C>T (p.Arg176Cys) rs757233968 0.00003
NM_001626.6(AKT2):c.169G>A (p.Val57Ile) rs1407888862 0.00002
NM_001626.6(AKT2):c.550C>T (p.Arg184Trp) rs752597471 0.00002
NM_001626.6(AKT2):c.1036G>A (p.Gly346Ser) rs1169786300 0.00001
NM_001626.6(AKT2):c.1069C>T (p.Arg357Cys) rs1026908617 0.00001
NM_001626.6(AKT2):c.1363C>T (p.Arg455Cys) rs757239082 0.00001
NM_001626.6(AKT2):c.268G>A (p.Val90Met) rs1160079555 0.00001
NM_001626.6(AKT2):c.337C>T (p.Arg113Trp) rs1054914884 0.00001
NM_001626.6(AKT2):c.757C>T (p.Arg253Trp) rs781527200 0.00001
NC_000019.9:g.(?_39205089)_(40913839_?)dup
NM_001626.6(AKT2):c.1032G>A (p.Met344Ile)
NM_001626.6(AKT2):c.1039C>T (p.Arg347Cys)
NM_001626.6(AKT2):c.1040G>A (p.Arg347His)
NM_001626.6(AKT2):c.1090A>G (p.Met364Val)
NM_001626.6(AKT2):c.1286A>G (p.Gln429Arg) rs1399189737
NM_001626.6(AKT2):c.136G>A (p.Asp46Asn) rs1975583524
NM_001626.6(AKT2):c.173C>T (p.Ala58Val) rs2145306024
NM_001626.6(AKT2):c.175+13A>G
NM_001626.6(AKT2):c.208C>G (p.Pro70Ala) rs1170693725
NM_001626.6(AKT2):c.282C>G (p.Asp94Glu) rs139125633
NM_001626.6(AKT2):c.283G>A (p.Glu95Lys)
NM_001626.6(AKT2):c.380C>T (p.Pro127Leu)
NM_001626.6(AKT2):c.401A>C (p.Glu134Ala)
NM_001626.6(AKT2):c.416C>T (p.Ala139Val)
NM_001626.6(AKT2):c.427G>A (p.Ala143Thr) rs2145207525
NM_001626.6(AKT2):c.430C>T (p.Arg144Trp)
NM_001626.6(AKT2):c.438A>G (p.Lys146=)
NM_001626.6(AKT2):c.44G>A (p.Arg15His) rs1976263420
NM_001626.6(AKT2):c.527G>T (p.Arg176Leu)
NM_001626.6(AKT2):c.572A>G (p.Lys191Arg)
NM_001626.6(AKT2):c.576T>G (p.Asp192Glu)
NM_001626.6(AKT2):c.641C>T (p.Ala214Val)
NM_001626.6(AKT2):c.709-3C>G
NM_001626.6(AKT2):c.709-3C>T
NM_001626.6(AKT2):c.960+3G>T rs56165898
NM_001626.6(AKT2):c.961-2dup

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