Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10096633 1.000 0.040 8 19973410 regulatory region variant C/T snv 0.22 8
rs10244051 1.000 0.080 7 15024208 intergenic variant T/A;G snv 3
rs10401969
SUGP1
0.776 0.240 19 19296909 intron variant T/C snv 0.10 25
rs10518693
IVD
15 40407823 intron variant C/T snv 0.37 2
rs10799701 1 21494497 intergenic variant A/G snv 0.47 2
rs10885409
TCF7L2
1.000 0.080 10 113048313 intron variant T/C snv 0.54 3
rs10965246 9 22132699 downstream gene variant T/C snv 0.15 2
rs11185790
PANK1
10 89612776 intron variant G/A snv 0.15 3
rs11705729
IGF2BP2
1.000 0.080 3 185789511 intron variant A/T snv 0.45 3
rs11924032
SLC2A2
3 171017310 intron variant G/A snv 0.29 3
rs1203936 20 22611792 upstream gene variant G/C;T snv 2
rs12053049
SPC25
2 168910638 intron variant T/C snv 5.2E-02 2
rs12310617 0.851 0.120 12 3060327 intergenic variant C/T snv 0.11 16
rs12369179
ZCCHC8
0.851 0.120 12 122479003 intron variant C/T snv 5.9E-02 16
rs12420422 0.851 0.120 11 123009573 intergenic variant G/A snv 3.4E-02 16
rs12579302
ATP2B1
0.851 0.120 12 89656726 intron variant A/G snv 0.15 19
rs1260326
GCKR
0.645 0.600 2 27508073 missense variant T/C;G snv 0.63; 4.0E-06 0.68 81
rs12670403
LOC101927609 ; AHR
7 17269655 intron variant C/A snv 0.46 2
rs12712928 2 44964941 intron variant G/C snv 0.18 2
rs12753193 1 65703996 non coding transcript exon variant G/A snv 0.58 3
rs13114738
SLC39A8
0.851 0.120 4 102363708 intron variant C/A;T snv 16
rs13266634
SLC30A8 ; LOC105375716
0.724 0.480 8 117172544 missense variant C/A;T snv 0.29 23
rs1333049
CDKN2B-AS1
0.614 0.520 9 22125504 intron variant G/C snv 0.41 60
rs13391552
ALMS1
2 73591809 intron variant G/A;C snv 2
rs1349497
RAPGEF4-AS1
2 172727935 intron variant G/A;C snv 2