Disease: Diabetes Mellitus
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1260326
GCKR
0.645 0.600 2 27508073 missense variant T/C;G snv 0.63; 4.0E-06 0.68 81
rs780094
GCKR
0.658 0.400 2 27518370 intron variant T/C snv 0.67 62
rs334
HBB
0.724 0.240 11 5227002 missense variant T/A;C;G snv 3.5E-03 35
rs1047891
CPS1
0.827 0.200 2 210675783 missense variant C/A snv 0.30 0.33 34
rs780093
GCKR
0.763 0.240 2 27519736 intron variant T/C snv 0.68 30
rs10224002
PRKAG2
0.925 0.080 7 151717955 intron variant A/G snv 0.31 12
rs12917707
UMOD
0.827 0.200 16 20356368 upstream gene variant G/T snv 0.14 11
rs550057
ABO
0.925 0.080 9 133271182 intron variant T/A;C snv 11
rs13333226
UMOD
0.827 0.200 16 20354332 intron variant A/G snv 0.23 10
rs10224210
PRKAG2
1.000 0.040 7 151716108 intron variant T/C snv 0.21 9
rs2079742
BCAS3
0.851 0.240 17 61388336 non coding transcript exon variant T/C snv 0.20 9
rs62435145 1.000 0.040 7 1246931 regulatory region variant G/T snv 0.51 8
rs963837
LOC101928338 ; LINC02859
0.925 0.120 11 30727543 intergenic variant T/C snv 0.35 8
rs11864909
PDILT
0.851 0.160 16 20389517 intron variant C/T snv 0.23 7
rs267734 0.925 0.120 1 150979001 upstream gene variant T/C snv 0.14 7
rs35789010
CARMIL1
0.851 0.200 6 25513951 intron variant G/A snv 4.1E-02 7
rs3765209
LOC101927745
0.851 0.040 21 15417030 intron variant C/T snv 0.31 7
rs13146355
SHROOM3
1.000 0.040 4 76490987 intron variant G/A snv 0.33 6
rs12922822
UMOD
1.000 0.040 16 20356323 upstream gene variant C/A;T snv 5
rs497309
CYP21A2 ; C2
0.882 0.240 6 31924707 intron variant A/C;G snv 5
rs8096658
NFATC1 ; LOC107985163
0.925 0.120 18 79396537 intron variant C/G snv 0.39 5
rs1264347
LINC00243
1.000 0.040 6 30830920 upstream gene variant C/T snv 7.9E-02 4
rs13191445 0.925 0.120 6 26015261 upstream gene variant G/A snv 5.6E-02 4
rs2517601
TRIM31-AS1 ; TRIM31
0.925 0.080 6 30106295 intron variant G/C snv 0.10 4
rs3812035
SLC34A1
1.000 0.040 5 177390142 3 prime UTR variant G/A;T snv 4