Source: GWASCAT

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs687621
ABO
0.851 0.240 9 133261662 intron variant G/A;C snv 11
rs11205303
MTMR11
0.882 0.120 1 149934520 missense variant T/C snv 0.33 0.29 8
rs6570507
ADGRG6
0.827 0.240 6 142358435 intron variant G/A snv 0.47 7
rs11157436
TRAV30
0.851 0.040 14 22168978 synonymous variant C/T snv 0.19 7
rs545608
CRYZL2P-SEC16B ; SEC16B
0.925 0.040 1 177929986 intron variant G/C snv 0.20 4
rs2816992
NR5A2 ; LOC107985244
0.925 0.040 1 200100088 intron variant A/G snv 0.39 4
rs10052657
PDE4D
0.807 0.120 5 59111944 intron variant C/A snv 0.17 4
rs11190870 0.827 0.200 10 101219450 intergenic variant T/A;C snv 3
rs6871087 0.925 0.040 5 30899410 intergenic variant A/G snv 8.5E-02 3
rs7741741
ADGRG6
0.925 0.040 6 142334664 intron variant T/A;G snv 3
rs9384713
AK9
0.882 0.080 6 109558038 intron variant G/T snv 0.57 3
rs12579350
ANO2
0.882 0.080 12 5687935 intron variant G/A snv 0.12 3
rs17694493
CDKN2B-AS1
0.882 0.120 9 22041999 intron variant C/G snv 0.12 3
rs4364959
DNAJC1
0.882 0.080 10 21996442 intron variant C/T snv 0.77 3
rs12149832
FTO
0.851 0.120 16 53808996 intron variant G/A snv 0.31 3
rs2145839
LOC105372648
0.925 0.040 20 48856501 regulatory region variant G/T snv 0.29 3
rs886448
LOC107986777
0.882 0.120 7 24200546 intron variant G/A snv 1.4E-03 3
rs10739217
LOC107987108
0.925 0.040 9 105973112 regulatory region variant T/A;C snv 3
rs1828853
MIR4300HG
0.925 0.040 11 82371520 intron variant G/A;C;T snv 3
rs1392817
PDE4B
0.925 0.040 1 66073773 intron variant A/G snv 0.51 3
rs7090135
RPS24
0.882 0.080 10 78043832 intron variant G/A;C snv 0.13 3
rs739496
SH2B3 ; ATXN2
0.790 0.160 12 111449855 3 prime UTR variant A/G snv 0.27 3
rs41520844
WRN
0.882 0.080 8 31135670 intron variant A/T snv 7.1E-02 3
rs10009128 0.925 0.040 4 19511508 intron variant C/T snv 0.34 2
rs10073216 0.925 0.040 5 169390084 intergenic variant A/G snv 5.1E-02 2