Source: GWASCAT

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs7890572
IL1RAPL1
X 29622701 intron variant A/G snv 9.3E-02 5
rs5942937 X 110473179 intron variant T/G snv 0.47 4
rs5985471 X 110460733 downstream gene variant C/T snv 0.43 4
rs138331350
FANCB
X 14841981 intron variant G/A snv 3.7E-02 1
rs2294915
PNPLA3
1.000 0.040 22 43945024 intron variant C/G;T snv 5
rs1811069
YDJC
1.000 0.040 22 21627765 upstream gene variant T/A;G snv 4
rs4820323
MAFF ; PLA2G6
22 38203760 non coding transcript exon variant C/A;G;T snv 4
rs133027
PLA2G6
22 38179492 intron variant T/- delins 0.46 2
rs181362
UBE2L3
22 21577779 intron variant C/T snv 0.31 2
rs4821116
UBE2L3
0.925 0.120 22 21619030 intron variant C/A;T snv 0.18 2
rs5754166
UBE2L3
0.925 0.160 22 21576488 intron variant C/T snv 0.18 2
rs7444
UBE2L3
1.000 0.080 22 21622645 3 prime UTR variant T/C snv 0.32 2
rs7445
UBE2L3
22 21622758 3 prime UTR variant C/G;T snv 0.22 2
rs147122512
SGSM3
22 40394561 intron variant G/A;C snv 1
rs181360
UBE2L3
22 21574627 intron variant T/G snv 0.21 1
rs2899297
PLA2G6
22 38198661 intron variant G/A snv 0.52 1
rs372767202 22 35363972 intergenic variant T/C snv 4.2E-05 1
rs5754344
UBE2L3
1.000 0.080 22 21609497 intron variant A/G snv 0.18 1
rs8135828
THOC5
22 29533250 intron variant G/A snv 0.14 1
rs8142788
ZNRF3
22 29004527 intron variant G/A snv 0.11 1
rs235314
PTTG1IP
21 44851537 missense variant C/T snv 0.48 0.46 3
rs496300
LINC01679
1.000 0.040 21 43359800 intron variant C/T snv 0.73 2
rs235374
PTTG1IP
21 44875071 upstream gene variant G/C snv 0.39 1
rs2834707
RUNX1
21 34971255 intron variant C/T snv 0.35 1
rs1800961
HNF4A
0.851 0.160 20 44413724 missense variant C/T snv 3.1E-02 2.5E-02 17