Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1229984
ADH1B
0.570 0.560 4 99318162 missense variant T/C;G snv 0.90 25
rs13107325
SLC39A8
0.776 0.520 4 102267552 missense variant C/A;T snv 4.0E-06; 4.5E-02 24
rs7137828
ATXN2
0.763 0.200 12 111494996 intron variant C/A;T snv 14
rs198851
H4C3
6 26104404 downstream gene variant T/A;C;G snv 11
rs1128249
COBLL1
1.000 0.080 2 164672114 intron variant G/C;T snv 9
rs2925979
CMIP
1.000 0.080 16 81501185 intron variant T/A;C snv 9
rs633185
ARHGAP42
0.925 0.080 11 100722807 intron variant G/A;C snv 8
rs13108218
HGFAC
4 3442204 intron variant A/G;T snv 7
rs2681492
ATP2B1
0.925 0.040 12 89619312 intron variant T/C;G snv 7
rs11591147
PCSK9
0.677 0.360 1 55039974 missense variant G/A;T snv 1.2E-02 6
rs1290784
MECOM
3 169379112 intron variant C/A;T snv 6
rs17035646
CASZ1
1 10736490 intron variant G/A;T snv 6
rs2521501
FES
0.925 0.080 15 90894158 intron variant A/C;T snv 6
rs4299376
LOC102725159 ; ABCG8
0.851 0.120 2 43845437 intron variant G/C;T snv 6
rs10184428 2 164155317 intron variant C/A;G snv 5
rs12978472
INSR
19 7257979 intron variant C/G;T snv 5
rs13149993 4 80237391 regulatory region variant G/A;C snv 5
rs2013002 12 111762346 intron variant T/A;C snv 5
rs9292468 5 32818967 intergenic variant T/A;C snv 5
rs10127775
GALNT2
1 230160042 intron variant A/G;T snv 4
rs11870935
KPNB1
17 47655239 intron variant G/A;C snv 4
rs1275984 2 26688641 upstream gene variant A/C;G snv 4
rs1495743 8 18415790 intergenic variant G/A;C snv 4
rs150844304
TP53BP1
15 43434427 intron variant A/C;G snv 4
rs1689040 12 89584456 intron variant C/G;T snv 4