Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs6108787 20 10986566 intron variant T/G snv 0.46 5
rs62434109
PLEKHG1
6 150654176 intron variant T/G snv 8.4E-02 5
rs604723
ARHGAP42
1.000 0.040 11 100739815 intron variant T/C snv 0.78 8
rs3753584
MTHFR ; CLCN6
0.827 0.080 1 11804529 5 prime UTR variant T/C snv 0.14 5
rs11024074
PLEKHA7
0.925 0.040 11 16895672 intron variant T/C snv 0.29 3
rs11867410
APOH
17 66231245 intron variant T/C snv 4.0E-02 3
rs13082711 3 27496418 intergenic variant T/C snv 0.16 3
rs1330225 1 106293321 intergenic variant T/C snv 0.38 3
rs17135875
FBXL13
7 102878584 intron variant T/C snv 0.24 3
rs7497026 15 74916208 downstream gene variant T/C snv 0.46 2
rs7622665
ULK4
1.000 0.160 3 41929251 intron variant T/C snv 0.67 2
rs3184504
SH2B3 ; ATXN2
0.572 0.600 12 111446804 missense variant T/A;C;G snv 0.67 61
rs198851
H4C3
6 26104404 downstream gene variant T/A;C;G snv 11
rs2013002 12 111762346 intron variant T/A;C snv 5
rs419076
MECOM
3 169383098 intron variant T/A;C snv 3
rs2306363
SIPA1
11 65638129 5 prime UTR variant G/T snv 0.15 7
rs4373814 10 18131043 intergenic variant G/C;T snv 3
rs1801253
ADRB1
0.683 0.440 10 114045297 missense variant G/C snv 0.74 0.69 6
rs1350193
CSK
15 74791940 intron variant G/C snv 0.67 2
rs17035646
CASZ1
1 10736490 intron variant G/A;T snv 6
rs1980235
LOC107984543
12 89717005 intron variant G/A;T snv 2
rs9815354
ULK4
0.925 0.160 3 41871159 intron variant G/A;T snv 1
rs633185
ARHGAP42
0.925 0.080 11 100722807 intron variant G/A;C snv 8
rs7922049
CABCOCO1
10 61702607 intron variant G/A;C snv 3
rs10255839
EVX1
7 27249498 intron variant G/A snv 0.87 6