Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs6127099 20 54114863 intergenic variant A/T snv 0.28 5
rs661171
ZC3H12C ; RDX
11 110145794 intron variant T/G snv 0.69 5
rs35194449 20 54125508 regulatory region variant C/T snv 0.20 1
rs4443100 22 23030688 intergenic variant G/C snv 0.74 1
rs481121 1 36737884 regulatory region variant G/A snv 0.48 1
rs73186030 3 122294618 downstream gene variant C/T snv 0.11 1
rs219779
CLDN14 ; LOC105369301
21 36461453 synonymous variant G/A snv 0.21 0.25 1
rs2931353
CLVS1
8 61236323 intron variant A/G;T snv 1
rs76615278
FKBP8
19 18543778 intron variant G/A snv 0.14 1
rs2024724
IFFO2
1 18910613 intron variant G/A snv 0.10 1
rs77178854
LOC105373572 ; DPP10
2 115738963 intron variant C/G snv 1.8E-02 1
rs1890709
LOC105378178
14 48632630 intergenic variant A/G;T snv 1
rs11099476
RASGEF1B
4 81564902 intron variant T/A snv 0.39 1
rs4074995
RGS14
5 177370342 intron variant G/A snv 0.23 1
rs16981087
RIN2 ; LOC107987276
20 19759310 intron variant G/C snv 0.19 1