Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs568645819
SBF2
11 10228118 intron variant TTGT/- delins 2
rs34858804
MITF
3 69756466 intron variant TT/-;T;TTT;TTTTTTTT delins 2
rs576195416
EGLN1
1 231374522 intron variant TT/-;T;TTT;TTTT;TTTTTTTTTTTT delins 1
rs495828 0.827 0.200 9 133279294 upstream gene variant T/G snv 0.81 24
rs2968478 16 88792238 intergenic variant T/G snv 0.61 4
rs1331309
HBS1L
6 135085040 intron variant T/G snv 0.19 2
rs56235845
RGS14
5 177371039 splice region variant T/G snv 0.36 0.42 2
rs1260326
GCKR
0.645 0.600 2 27508073 missense variant T/C;G snv 0.63; 4.0E-06 0.68 81
rs62160676
MIR4435-2HG
2 111410354 intron variant T/C;G snv 5
rs780094
GCKR
0.658 0.400 2 27518370 intron variant T/C snv 0.67 62
rs174547
FADS2 ; FADS1
0.742 0.240 11 61803311 intron variant T/C snv 0.28 33
rs10401969
SUGP1
0.776 0.240 19 19296909 intron variant T/C snv 0.10 25
rs2074755
BAZ1B
0.807 0.240 7 73462836 non coding transcript exon variant T/C snv 9.2E-02 20
rs222826 0.851 0.120 2 146120964 regulatory region variant T/C snv 0.94 16
rs2519093
ABO
0.882 0.200 9 133266456 intron variant T/C snv 16
rs6533530 0.851 0.120 4 110810780 intergenic variant T/C snv 0.47 16
rs833070
VEGFA
0.776 0.440 6 43774889 non coding transcript exon variant T/C snv 0.58 11
rs12509595 1.000 0.080 4 80261400 intergenic variant T/C snv 0.23 10
rs10224210
PRKAG2
1.000 0.040 7 151716108 intron variant T/C snv 0.21 9
rs17476364
HK1
10 69334748 intron variant T/C snv 6.4E-02 8
rs9376090
HBS1L
6 135090090 intron variant T/C snv 0.19 7
rs2413450
TMPRSS6
22 37074184 intron variant T/C snv 0.61 6
rs128494
CLDN14 ; LOC105369301
21 36461960 intron variant T/C snv 0.72 4
rs8069437
LRRC37A2 ; WNT3
17 46829583 intron variant T/C snv 0.82 4
rs9483788 6 135114363 intergenic variant T/C snv 0.19 4