Source: GWASCAT

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs17693963 0.882 0.040 6 27742386 upstream gene variant A/C;G snv 3
rs221798
GIGYF1
0.882 0.040 7 100689872 intron variant C/A;G snv 3
rs2535627 1.000 0.040 3 52811089 downstream gene variant T/A;C;G snv 3
rs268134
SPRED2
0.925 0.120 2 65381229 intron variant A/C;G;T snv 3
rs28437878
HYKK
1.000 0.040 15 78515530 intron variant C/G;T snv 3
rs3747631
LOC105371692 ; LRRN2
1.000 0.040 1 204618441 missense variant G/A;C snv 4.0E-06; 0.20 3
rs4664442
SLC4A10
1.000 0.040 2 161971491 intron variant G/A;C snv 3
rs4702
FES ; FURIN
1.000 0.040 15 90883330 3 prime UTR variant G/A;C snv 3
rs6558872
CSMD1
0.882 0.040 8 4380617 intron variant G/A;C snv 3
rs6712515
AFF3
0.925 0.160 2 100190052 intron variant T/A;C snv 3
rs72986630
ZNF823
1.000 0.040 19 11738921 5 prime UTR variant C/A;T snv 3
rs7405404 0.925 0.040 16 13656002 intergenic variant T/A;C snv 3
rs7766730 0.882 0.040 6 65987110 intergenic variant C/A;T snv 3
rs9556958
FARP1 ; STK24
1.000 0.040 13 98447792 3 prime UTR variant C/G;T snv 3
rs9636107
TCF4
1.000 0.040 18 55532886 intron variant A/G;T snv 3
rs10061788
LINC00461
1.000 0.040 5 88638889 intron variant G/A;T snv 2
rs1024582
CACNA1C
1.000 0.040 12 2293080 intron variant A/G;T snv 2
rs10520163
CLCN3
1.000 0.040 4 169705401 intron variant T/A;C snv 2
rs10757417 1.000 0.040 9 23347855 intron variant G/A;T snv 2
rs1076884 1.000 0.040 16 13653946 intergenic variant C/G;T snv 2
rs10961430
NFIB
1.000 0.040 9 14224064 intron variant G/C;T snv 2
rs11130
NDE1 ; MYH11
1.000 0.040 16 15724453 3 prime UTR variant G/A;C snv 0.56; 4.0E-06 2
rs111312615
HLA-A
1.000 0.040 6 29955302 upstream gene variant T/G snv 2
rs11166628
LINC02055
1.000 0.040 8 136066082 intron variant G/A;C snv 2
rs111977918
HLA-C
1.000 0.040 6 31268274 downstream gene variant G/A;C snv 2