Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1800795
IL6-AS1 ; IL6 ; STEAP1B
0.494 0.840 7 22727026 intron variant C/G snv 0.71 1
rs1815739
ACTN3
0.763 0.240 11 66560624 stop gained C/T snv 0.37 1
rs10830963
MTNR1B
0.776 0.400 11 92975544 intron variant C/G snv 0.22 7
rs739496
SH2B3 ; ATXN2
0.790 0.160 12 111449855 3 prime UTR variant A/G snv 0.27 3
rs10052657
PDE4D
0.807 0.120 5 59111944 intron variant C/A snv 0.17 4
rs6570507
ADGRG6
0.827 0.240 6 142358435 intron variant G/A snv 0.47 7
rs11190870 0.827 0.200 10 101219450 intergenic variant T/A;C snv 3
rs10489629
IL23R ; C1orf141
0.827 0.240 1 67222666 intron variant T/C snv 0.48 2
rs6137473 0.827 0.280 20 21904055 intergenic variant G/A snv 0.61 2
rs687621
ABO
0.851 0.240 9 133261662 intron variant G/A;C snv 11
rs11157436
TRAV30
0.851 0.040 14 22168978 synonymous variant C/T snv 0.19 7
rs12149832
FTO
0.851 0.120 16 53808996 intron variant G/A snv 0.31 3
rs1254900
VAMP5
0.851 0.120 2 85589211 intron variant A/G snv 0.81 2
rs2384506 0.851 0.080 12 114991548 intergenic variant T/C snv 0.21 2
rs678741
LBX1-AS1
0.851 0.200 10 101237824 intron variant G/A snv 0.51 2
rs11205303
MTMR11
0.882 0.120 1 149934520 missense variant T/C snv 0.33 0.29 8
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
rs41520844
WRN
0.882 0.080 8 31135670 intron variant A/T snv 7.1E-02 3
rs4364959
DNAJC1
0.882 0.080 10 21996442 intron variant C/T snv 0.77 3
rs7090135
RPS24
0.882 0.080 10 78043832 intron variant G/A;C snv 0.13 3
rs886448
LOC107986777
0.882 0.120 7 24200546 intron variant G/A snv 1.4E-03 3
rs9384713
AK9
0.882 0.080 6 109558038 intron variant G/T snv 0.57 3
rs1086603 0.882 0.120 1 147816164 intergenic variant G/A snv 3.4E-02 2
rs12289095
PRCP
0.882 0.120 11 82858764 5 prime UTR variant G/A snv 0.13 2