Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1004446
IGF2 ; INS-IGF2 ; IGF2-AS
0.827 0.240 11 2148913 intron variant G/A snv 0.37 3
rs10402271 1.000 0.080 19 44825957 downstream gene variant T/G snv 0.28 6
rs1048699
PPP1R37 ; MARK4
1.000 0.080 19 45147128 3 prime UTR variant C/T snv 9.0E-02 2
rs11136000
CLU
0.752 0.160 8 27607002 intron variant T/C snv 0.56 3
rs1114832
PPP1R37 ; MARK4
1.000 0.080 19 45132943 intron variant C/T snv 9.2E-02 2
rs11755527
BACH2
0.851 0.360 6 90248512 intron variant C/G snv 0.36 3
rs11894266 1.000 0.080 2 169780132 downstream gene variant C/T snv 0.45 2
rs12518099
LINC01339
0.925 0.120 5 90250292 intron variant A/G;T snv 3
rs12610605
NECTIN2
1.000 0.080 19 44867581 intron variant G/A snv 0.15 2
rs12708716
CLEC16A
0.807 0.320 16 11086016 intron variant A/G snv 0.37 4
rs12722495
IL2RA
0.851 0.200 10 6055320 intron variant T/C snv 7.0E-02 1
rs13266634
SLC30A8 ; LOC105375716
0.724 0.480 8 117172544 missense variant C/A;T snv 0.29 3
rs157580
TOMM40
0.882 0.160 19 44892009 intron variant G/A snv 0.69 11
rs1701704
LOC105369781 ; IKZF4
0.851 0.200 12 56018703 intron variant T/G snv 0.25 5
rs1871047
NECTIN2
1.000 0.080 19 44848489 intron variant A/G snv 0.31 2
rs1990760
IFIH1
0.672 0.480 2 162267541 missense variant C/T snv 0.50 0.45 4
rs2069762
IL2
0.672 0.560 4 122456825 upstream gene variant A/C snv 0.24 1
rs2075650
TOMM40
0.662 0.360 19 44892362 intron variant A/G snv 0.13 0.13 20
rs2292239
ERBB3
0.742 0.480 12 56088396 intron variant T/G snv 0.65 4
rs2304256
TYK2
0.732 0.360 19 10364976 missense variant C/A snv 0.27 0.23 3
rs2476601
AP4B1-AS1 ; PTPN22
0.498 0.800 1 113834946 missense variant A/G snv 0.93 0.93 13
rs2542151 0.763 0.480 18 12779948 upstream gene variant G/T snv 0.83 6
rs2582367 1.000 0.080 8 27622508 regulatory region variant C/T snv 0.64 2
rs2927438 0.925 0.080 19 44738850 intergenic variant G/A snv 0.20 5
rs2943641 0.763 0.160 2 226229029 intergenic variant T/C snv 0.67 3