Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2395029
HCP5
0.790 0.320 6 31464003 non coding transcript exon variant T/G snv 2.7E-02 2.4E-02 7
rs3815087
PSORS1C1
0.851 0.200 6 31125810 5 prime UTR variant G/A snv 0.25 6
rs8321
ZNRD1
0.742 0.320 6 30064745 3 prime UTR variant A/C snv 5.4E-02 5.9E-02 6
rs3732378
CX3CR1
0.620 0.720 3 39265671 missense variant G/A snv 0.14 0.12 4
rs7756521
DDR1
1.000 6 30880476 intron variant T/C snv 0.25 4
rs9368699
SNHG32 ; SNORD48
0.851 0.200 6 31834764 non coding transcript exon variant T/C snv 3.2E-02 4
rs1799864
CCR2
0.572 0.680 3 46357717 missense variant G/A snv 0.13 0.12 2
rs1800871
IL19 ; IL10
0.508 0.800 1 206773289 5 prime UTR variant A/G snv 0.69 2
rs10484554
LOC112267902 ; HLA-B
0.807 0.200 6 31306778 intron variant C/T snv 0.12 2
rs3823418
PSORS1C1
0.925 0.120 6 31133165 intron variant G/A snv 0.23 2
rs13194504 0.925 0.120 6 28662914 intergenic variant G/A snv 5.1E-02 1
rs2248462 0.807 0.240 6 31479019 downstream gene variant G/A snv 0.19 1
rs4118325 1 107035210 intergenic variant G/A;T snv 1
rs4324798 0.790 0.240 6 28808340 intergenic variant G/A snv 7.2E-02 1
rs6467710
DGKI
7 137519073 intron variant G/A;C snv 1
rs2894207
LINC02571 ; HLA-B
0.882 0.160 6 31295974 intron variant T/C snv 0.20 1
rs3749971
OR12D3 ; OR5V1
0.925 0.160 6 29374998 missense variant G/A snv 5.5E-02 5.7E-02 1
rs11884476
PARD3B
2 205453869 intron variant C/G snv 0.11 1