Source: GWASCAT

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs7933433 0.827 0.120 11 128324555 intergenic variant G/T snv 0.42 5
rs7915475
ZNF365
0.827 0.120 10 62621908 intron variant A/G snv 0.28 5
rs78973538
GBAP1
0.827 0.120 1 155224224 intron variant C/T snv 4.8E-03 5
rs7848647
TNFSF15
0.732 0.320 9 114806766 upstream gene variant T/C snv 0.74 6
rs7831697 0.724 0.240 8 137124061 regulatory region variant T/A;C;G snv 14
rs7805114 0.827 0.120 7 107809588 downstream gene variant T/A;G snv 5
rs77981966
THADA
0.827 0.120 2 43550825 intron variant C/T snv 4.6E-02 5
rs7743761 1.000 0.040 6 31368323 intron variant C/A snv 0.31 1
rs7731626
ANKRD55
0.716 0.240 5 56148856 intron variant G/A snv 0.30 15
rs7725052 0.716 0.240 5 40487168 intron variant C/T snv 0.52 15
rs77150043
ADCY7
0.724 0.240 16 50270338 intron variant C/T snv 0.17 14
rs769178 1.000 0.040 6 31579737 downstream gene variant G/T snv 8.3E-02 1
rs76913543 0.827 0.120 10 6000052 intergenic variant G/A;C snv 5
rs7672495 0.724 0.240 4 4990640 regulatory region variant T/C snv 0.21 14
rs7660520 0.724 0.240 4 182824168 upstream gene variant G/A;C snv 14
rs76418789
IL23R ; C1orf141
0.882 0.080 1 67182913 missense variant G/A snv 7.3E-03 4.5E-03 2
rs763780
IL17F
0.531 0.720 6 52236941 missense variant T/C snv 6.7E-02 6.6E-02 1
rs7608910
PUS10
0.827 0.120 2 60977721 intron variant A/G snv 0.37 6
rs7574865
STAT4
0.574 0.720 2 191099907 intron variant T/G snv 0.79 9
rs7556897 0.807 0.120 2 227795396 intergenic variant C/G;T snv 6
rs755374 0.724 0.240 5 159402286 intron variant C/T snv 0.28 14
rs7552167 0.807 0.120 1 24192153 upstream gene variant A/G snv 0.87 6
rs7517847
IL23R ; C1orf141
0.689 0.600 1 67215986 intron variant T/G snv 0.37 5
rs74956615
FDX2 ; RAVER1
0.807 0.160 19 10317045 3 prime UTR variant T/A;C snv 5
rs74817271
TNIP1
0.807 0.120 5 151090412 intron variant G/A snv 5.0E-02 6