Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs657152
ABO
0.882 0.200 9 133263862 intron variant A/C;T snv 14
rs9472138
LOC107986598
0.882 0.160 6 43844025 downstream gene variant C/T snv 0.24 5
rs17277546
TRIM4
7 99891948 3 prime UTR variant G/A snv 3.1E-02 3
rs2497304 1.000 0.080 10 92732959 intergenic variant C/T snv 0.36 2
rs2235544
DIO1
0.742 0.240 1 53909897 intron variant C/A;T snv 0.53; 4.0E-06 2
rs3813582
LINC01229 ; LOC105371356 ; MAFTRR
16 79715456 non coding transcript exon variant T/C snv 0.28 2
rs10799824
LOC105376819 ; LOC105376817 ; MICOS10
1 19514680 intron variant G/A snv 0.18 2
rs10032216
LOC107986195
4 148748354 intron variant T/A;C snv 2
rs6885099
PDE8B
1.000 0.040 5 77234524 intron variant A/G snv 0.52 2
rs4924410
SRP14-AS1
1.000 0.040 15 40047293 intron variant A/C snv 0.73 2
rs8026641
SRP14-AS1
1.000 0.040 15 40046660 intron variant G/A snv 0.73 2
rs11761528
ZKSCAN5
1.000 0.120 7 99521178 intron variant C/T snv 0.12 2
rs1017993 19 47900919 intergenic variant C/T snv 0.11 1
rs10278040 7 99543750 downstream gene variant G/A snv 0.16 1
rs10410350 19 47849107 regulatory region variant A/G snv 0.18 1
rs10744816 12 114276461 regulatory region variant T/C snv 0.39 1
rs11624776 14 93129246 regulatory region variant A/C;T snv 1
rs11726248 4 170132368 intergenic variant G/A snv 6.8E-02 1
rs1624802 12 130012927 intergenic variant A/G;T snv 1
rs16981893 19 47961868 intergenic variant G/A snv 0.22 1
rs17272617 19 47854103 intergenic variant G/A snv 0.12 1
rs17776563 15 88575873 intergenic variant G/A;C snv 1
rs182421 19 47900226 intergenic variant A/G snv 0.11 1
rs2488073 10 92739218 intergenic variant A/G snv 0.42 1
rs2488075 10 92730417 regulatory region variant T/C snv 0.40 1