Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2075650
TOMM40
0.662 0.360 19 44892362 intron variant A/G snv 0.13 0.13 20
rs657152
ABO
0.882 0.200 9 133263862 intron variant A/C;T snv 14
rs157580
TOMM40
0.882 0.160 19 44892009 intron variant G/A snv 0.69 11
rs7903146
TCF7L2
0.554 0.680 10 112998590 intron variant C/G;T snv 8
rs1701704
LOC105369781 ; IKZF4
0.851 0.200 12 56018703 intron variant T/G snv 0.25 5
rs12708716
CLEC16A
0.807 0.320 16 11086016 intron variant A/G snv 0.37 4
rs2292239
ERBB3
0.742 0.480 12 56088396 intron variant T/G snv 0.65 4
rs8106922
TOMM40
1.000 0.080 19 44898409 intron variant A/G snv 0.36 4
rs1004446
IGF2 ; INS-IGF2 ; IGF2-AS
0.827 0.240 11 2148913 intron variant G/A snv 0.37 3
rs11136000
CLU
0.752 0.160 8 27607002 intron variant T/C snv 0.56 3
rs11755527
BACH2
0.851 0.360 6 90248512 intron variant C/G snv 0.36 3
rs12518099
LINC01339
0.925 0.120 5 90250292 intron variant A/G;T snv 3
rs4712523
CDKAL1
0.925 0.120 6 20657333 intron variant A/G snv 0.41 3
rs1114832
PPP1R37 ; MARK4
1.000 0.080 19 45132943 intron variant C/T snv 9.2E-02 2
rs12610605
NECTIN2
1.000 0.080 19 44867581 intron variant G/A snv 0.15 2
rs1871047
NECTIN2
1.000 0.080 19 44848489 intron variant A/G snv 0.31 2
rs377702
NECTIN2
1.000 0.080 19 44859410 intron variant G/A snv 0.34 2
rs8103315
BCL3
1.000 0.080 19 44750911 intron variant C/A snv 9.1E-02 2
rs12722495
IL2RA
0.851 0.200 10 6055320 intron variant T/C snv 7.0E-02 1
rs3788013
UBASH3A
0.851 0.240 21 42421219 intron variant C/A snv 0.44 1
rs2965101 1.000 0.080 19 44734556 intergenic variant T/C snv 0.34 6
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
rs7171171
LOC107984725
0.925 0.120 15 38614840 intergenic variant A/G snv 0.24 1
rs7941541 11 86147496 intergenic variant G/A snv 0.73 1