ClinVar Miner

List of variants reported as likely benign 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: 57
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HGVS dbSNP gnomAD frequency
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.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.1023C>T (p.Tyr341=) rs147634759 0.00006
NM_001626.6(AKT2):c.442-12T>C rs773981622 0.00005
NM_001626.6(AKT2):c.708+9C>T rs377332467 0.00004
NM_001626.6(AKT2):c.288-17C>T rs373327049 0.00003
NM_001626.6(AKT2):c.573+8C>T rs200843500 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.126C>T (p.Pro42=) rs1347826243 0.00001
NM_001626.6(AKT2):c.1413C>G (p.Pro471=) rs199536208 0.00001
NM_001626.6(AKT2):c.288-6G>C rs189986892 0.00001
NM_001626.6(AKT2):c.39C>T (p.His13=) rs1299106420 0.00001
NM_001626.6(AKT2):c.832-7C>T rs536687170 0.00001
NM_001626.6(AKT2):c.1068G>A (p.Glu356=)
NM_001626.6(AKT2):c.1110G>A (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.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.168C>T (p.Ser56=)
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.387C>T (p.Asp129=)
NM_001626.6(AKT2):c.399T>G (p.Thr133=) rs1599984715
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.574-15G>A
NM_001626.6(AKT2):c.574-16C>T
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.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.709-9C>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.990C>T (p.Ala330=)

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