Disease: Diabetes
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs13447075
PVT1
0.882 0.120 8 127998344 non coding transcript exon variant C/A snv 4
rs13333226
UMOD
0.827 0.200 16 20354332 intron variant A/G snv 0.23 10
rs12917707
UMOD
0.827 0.200 16 20356368 upstream gene variant G/T snv 0.14 11
rs1267969615
ACE
0.532 0.760 17 63490960 missense variant T/C snv 4.0E-06 100
rs1260326
GCKR
0.645 0.600 2 27508073 missense variant T/C;G snv 0.63; 4.0E-06 0.68 81
rs12513649 0.851 0.160 5 173045049 regulatory region variant C/G;T snv 6
rs1232898090
PPARA
0.637 0.600 22 46198429 missense variant G/C;T snv 4.0E-06; 4.0E-06 40
rs1217691063
MTHFR
0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs1188383936
F2
0.524 0.760 11 46725976 missense variant C/T snv 8.0E-06 102
rs11864909
PDILT
0.851 0.160 16 20389517 intron variant C/T snv 0.23 7
rs11622435
LOC101928462
0.827 0.120 14 81151652 intron variant G/A snv 4.7E-02 7
rs10887800
LOC101929727 ; RNLS
0.790 0.280 10 88316086 intron variant A/G;T snv 11
rs1061170
CFH
0.561 0.720 1 196690107 missense variant C/T snv 0.68 0.64 72
rs1047891
CPS1
0.827 0.200 2 210675783 missense variant C/A snv 0.30 0.33 34
rs1044498
ENPP1
0.752 0.360 6 131851228 missense variant A/C;G snv 0.19 15
rs1042713
ADRB2
0.576 0.800 5 148826877 missense variant G/A snv 0.42 0.43 63
rs1024611 0.568 0.800 17 34252769 upstream gene variant A/G snv 0.28 63