ClinVar Miner

List of variants studied 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: 113
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HGVS dbSNP gnomAD frequency
NM_001626.6(AKT2):c.1176-17C>T rs3730264 0.01279
NM_001626.6(AKT2):c.442-20A>G rs3730257 0.00355
NM_001626.6(AKT2):c.93C>T (p.Ser31=) rs35588791 0.00270
NM_001626.6(AKT2):c.573+9C>T rs3730258 0.00267
NM_001626.6(AKT2):c.945G>A (p.Glu315=) rs150000674 0.00174
NM_001626.6(AKT2):c.831+18C>T rs200438281 0.00146
NM_001626.6(AKT2):c.288-18dup rs371077077 0.00135
NM_001626.6(AKT2):c.1367-7C>T rs191069336 0.00063
NM_001626.6(AKT2):c.442-8C>T rs201884933 0.00059
NM_001626.6(AKT2):c.282C>T (p.Asp94=) rs139125633 0.00051
NM_001626.6(AKT2):c.960+3G>A rs56165898 0.00048
NM_001626.6(AKT2):c.1366+20G>A rs375549081 0.00042
NM_001626.6(AKT2):c.204G>A (p.Pro68=) rs139479466 0.00036
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.212A>G (p.Asn71Ser) rs200272953 0.00028
NM_001626.6(AKT2):c.961-13C>T rs367671463 0.00024
NM_001626.6(AKT2):c.1176-12G>A rs371347299 0.00019
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.1023C>T (p.Tyr341=) rs147634759 0.00006
NM_001626.6(AKT2):c.395C>T (p.Thr132Met) rs143335817 0.00005
NM_001626.6(AKT2):c.442-12T>C rs773981622 0.00005
NM_001626.6(AKT2):c.1296C>T (p.Ser432=) rs56098986 0.00004
NM_001626.6(AKT2):c.19A>G (p.Ile7Val) rs199748431 0.00004
NM_001626.6(AKT2):c.708+9C>T rs377332467 0.00004
NM_001626.6(AKT2):c.1112G>A (p.Arg371His) rs778561687 0.00003
NM_001626.6(AKT2):c.288-17C>T rs373327049 0.00003
NM_001626.6(AKT2):c.526C>T (p.Arg176Cys) rs757233968 0.00003
NM_001626.6(AKT2):c.573+8C>T rs200843500 0.00003
NM_001626.6(AKT2):c.666C>T (p.His222=) rs199761368 0.00003
NM_001626.6(AKT2):c.699C>T (p.Asn233=) rs765477884 0.00003
NM_001626.6(AKT2):c.711G>C (p.Leu237=) rs776435289 0.00003
NM_001626.6(AKT2):c.1065C>T (p.His355=) rs781682925 0.00002
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.126C>T (p.Pro42=) rs1347826243 0.00001
NM_001626.6(AKT2):c.1363C>T (p.Arg455Cys) rs757239082 0.00001
NM_001626.6(AKT2):c.1413C>G (p.Pro471=) rs199536208 0.00001
NM_001626.6(AKT2):c.268G>A (p.Val90Met) rs1160079555 0.00001
NM_001626.6(AKT2):c.288-6G>C rs189986892 0.00001
NM_001626.6(AKT2):c.337C>T (p.Arg113Trp) rs1054914884 0.00001
NM_001626.6(AKT2):c.39C>T (p.His13=) rs1299106420 0.00001
NM_001626.6(AKT2):c.757C>T (p.Arg253Trp) rs781527200 0.00001
NM_001626.6(AKT2):c.832-7C>T rs536687170 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.1068G>A (p.Glu356=)
NM_001626.6(AKT2):c.1090A>G (p.Met364Val)
NM_001626.6(AKT2):c.1110G>A (p.Pro370=) rs41309435
NM_001626.6(AKT2):c.1110G>T (p.Pro370=) rs41309435
NM_001626.6(AKT2):c.1125C>T (p.Pro375=)
NM_001626.6(AKT2):c.1176-10C>G rs2145160063
NM_001626.6(AKT2):c.1227C>T (p.Phe409=)
NM_001626.6(AKT2):c.1264-4G>A
NM_001626.6(AKT2):c.1264-4G>T rs763704160
NM_001626.6(AKT2):c.1286A>G (p.Gln429Arg) rs1399189737
NM_001626.6(AKT2):c.1311G>A (p.Arg437=)
NM_001626.6(AKT2):c.132C>T (p.Ala44=) rs962740719
NM_001626.6(AKT2):c.1366+19C>T
NM_001626.6(AKT2):c.136G>A (p.Asp46Asn) rs1975583524
NM_001626.6(AKT2):c.168C>T (p.Ser56=)
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.288-14G>T
NM_001626.6(AKT2):c.288-8C>T rs1335755410
NM_001626.6(AKT2):c.318C>T (p.Val106=) rs769503941
NM_001626.6(AKT2):c.327C>T (p.Ser109=)
NM_001626.6(AKT2):c.380C>T (p.Pro127Leu)
NM_001626.6(AKT2):c.387C>T (p.Asp129=)
NM_001626.6(AKT2):c.399T>G (p.Thr133=) rs1599984715
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.46+10C>T
NM_001626.6(AKT2):c.46+20C>T
NM_001626.6(AKT2):c.525C>T (p.Gly175=) rs1209741122
NM_001626.6(AKT2):c.527G>T (p.Arg176Leu)
NM_001626.6(AKT2):c.572A>G (p.Lys191Arg)
NM_001626.6(AKT2):c.574-15G>A
NM_001626.6(AKT2):c.574-16C>T
NM_001626.6(AKT2):c.576T>G (p.Asp192Glu)
NM_001626.6(AKT2):c.582C>T (p.Val194=)
NM_001626.6(AKT2):c.597C>T (p.Thr199=)
NM_001626.6(AKT2):c.639+11C>G
NM_001626.6(AKT2):c.640-20C>T
NM_001626.6(AKT2):c.641C>T (p.Ala214Val)
NM_001626.6(AKT2):c.708+19_708+20insGCGGCTGCCTTGGCT rs1369307021
NM_001626.6(AKT2):c.708+8G>A
NM_001626.6(AKT2):c.709-11T>A
NM_001626.6(AKT2):c.709-14C>T
NM_001626.6(AKT2):c.709-3C>G
NM_001626.6(AKT2):c.709-3C>T
NM_001626.6(AKT2):c.709-9C>T rs2145179062
NM_001626.6(AKT2):c.792G>A (p.Glu264=)
NM_001626.6(AKT2):c.822C>G (p.Arg274=)
NM_001626.6(AKT2):c.822C>T (p.Arg274=) rs758906645
NM_001626.6(AKT2):c.831+10A>G rs2145177700
NM_001626.6(AKT2):c.831+4A>G
NM_001626.6(AKT2):c.960+20G>T
NM_001626.6(AKT2):c.960+3G>T rs56165898
NM_001626.6(AKT2):c.961-2dup
NM_001626.6(AKT2):c.990C>T (p.Ala330=)

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