ClinVar Miner

List of variants reported as benign for Type 2 diabetes mellitus

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Total variants: 69
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HGVS dbSNP gnomAD frequency
NM_002711.4(PPP1R3A):c.1428T>A (p.Asn476Lys) rs2974944 0.99641
NM_002711.4(PPP1R3A):c.1351G>A (p.Val451Met) rs2974942 0.97316
NM_002711.4(PPP1R3A):c.2645T>A (p.Leu882His) rs2974938 0.97161
NM_000207.3(INS):c.187+11T>C rs5506 0.93263
NM_001371909.1(C10orf67):c.910-1375T>G rs4454613 0.84565
NM_002999.4(SDC4):c.445+251C>T rs2425696 0.75835
NM_001366110.1(PAX4):c.986A>C (p.His329Pro) rs712701 0.74681
NM_001366110.1(PAX4):c.*211A>G rs712700 0.74585
NM_000525.4(KCNJ11):c.67A>G (p.Lys23Glu) rs5219 0.72048
NM_000352.6(ABCC8):c.4105G>T (p.Ala1369Ser) rs757110 0.71935
NM_015874.6(RBPJ):c.20+29693T>G rs6853254 0.70332
NM_001371909.1(C10orf67):c.1201-4652A>G rs7904665 0.59355
NC_000004.12:g.26444384G>A rs2788865 0.59299
NC_000004.12:g.26450075G>A rs13116206 0.56404
NM_015874.6(RBPJ):c.21-2640G>A rs7655165 0.56073
NM_015874.6(RBPJ):c.20+13573C>T rs13144326 0.52441
NM_001001547.3(CD36):c.-184+13244G>A rs1761667 0.49113
NM_002999.4(SDC4):c.199+134A>G rs2072792 0.48742
NM_015874.6(RBPJ):c.156-2327G>C rs12639629 0.48387
NC_000010.11:g.23177805G>A rs7916519 0.48352
NC_000020.11:g.45324436T>G rs720063 0.44729
NM_000525.4(KCNJ11):c.*215C>T rs5210 0.44390
NM_000352.6(ABCC8):c.3819G>A (p.Arg1273=) rs1799859 0.39734
NM_000545.8(HNF1A):c.79A>C (p.Ile27Leu) rs1169288 0.35489
NM_015874.6(RBPJ):c.60-5130C>T rs12650452 0.34910
NM_006208.3(ENPP1):c.517A>C (p.Lys173Gln) rs1044498 0.32168
NM_022895.3(C12orf43):c.*2523C>T rs1169310 0.30485
NM_002999.4(SDC4):c.446-1455C>T rs985586 0.26964
NM_000545.8(HNF1A):c.1460G>A (p.Ser487Asn) rs2464196 0.26206
NM_000545.8(HNF1A):c.1375C>T (p.Leu459=) rs2259820 0.26141
NC_000020.11:g.45319581A>C rs11698812 0.24897
NC_000010.11:g.23163713A>G rs10741021 0.23437
NM_000340.2(SLC2A2):c.776-15C>T rs5406 0.21500
NM_001371909.1(C10orf67):c.851-537C>T rs7090683 0.19272
NM_000340.2(SLC2A2):c.594G>A (p.Thr198=) rs5404 0.15665
NM_001001548.3(CD36):c.281+924C>A rs3211867 0.14236
NM_015874.6(RBPJ):c.321+406G>A rs79533922 0.10243
NM_003064.4(SLPI):c.85+267C>T rs59339622 0.09487
NC_000010.11:g.23189850T>G rs4748844 0.08608
NM_000352.6(ABCC8):c.330C>T (p.Ala110=) rs8192695 0.06691
NC_000020.11:g.45279237T>C rs79312216 0.05422
NM_014276.4(RBPJL):c.132-389T>C rs2076027 0.04512
NM_014276.4(RBPJL):c.759T>C (p.Ala253=) rs2076026 0.03721
NM_015874.6(RBPJ):c.21-26407G>A rs73245775 0.02770
NM_175914.5(HNF4A):c.350C>T (p.Thr117Ile) rs1800961 0.02469
NM_000525.4(KCNJ11):c.801C>G (p.Leu267=) rs5216 0.01521
NM_005544.3(IRS1):c.1534G>C (p.Ala512Pro) rs1801276 0.01357
NM_005349.3(RBPJ):c.-1504G>A rs186895314 0.00771
NM_000160.5(GCGR):c.118G>A (p.Gly40Ser) rs1801483 0.00636
NM_015874.6(RBPJ):c.20+10722T>G rs78445835 0.00557
NC_000004.12:g.26222167C>T rs114530054 0.00396
NC_000010.11:g.23167584A>C rs16923098 0.00379
NC_000020.11:g.45157150A>G rs143311170 0.00366
NM_002999.4(SDC4):c.61-965T>C rs147593522 0.00361
NM_014276.4(RBPJL):c.23-481C>G rs138228405 0.00354
NM_000209.4(PDX1):c.226G>A (p.Asp76Asn) rs137852783 0.00320
NM_015874.6(RBPJ):c.21-20856T>C rs78672655 0.00312
NM_001371909.1(C10orf67):c.1200+6658G>T rs116846325 0.00248
NM_015874.4(RBPJ):c.-112G>A rs185848565 0.00141
NM_015874.6(RBPJ):c.59+2331A>C rs186035024 0.00051
NC_000010.11:g.23187502G>A rs187391034 0.00038
NM_000525.4(KCNJ11):c.852C>A (p.Ile284=) rs1800854 0.00038
NC_000004.12:g.26453607G>C rs930109604 0.00021
NM_001393530.1(MATN4):c.643+703C>T rs961418965 0.00005
NC_000020.11:g.45324681_45324682del rs33961254
NM_001371909.1(C10orf67):c.1434+6169G>A rs1554804525
NM_002999.4(SDC4):c.61-4447del rs148973596
NM_014276.4(RBPJL):c.1333G>A (p.Asp445Asn) rs1555859311
NM_015874.6(RBPJ):c.60-8189dup rs77056130

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