Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2074480
RNF39
1.000 6 30073033 intron variant T/G snv 0.17 4
rs2074479
RNF39
1.000 6 30073232 missense variant A/G snv 0.15 0.17 4
rs2844795
TRIM31 ; TRIM31-AS1
0.925 0.120 6 30106070 intron variant C/G;T snv 5
rs9468692
TRIM10
1.000 6 30152113 3 prime UTR variant G/A;C;T snv 4
rs2072107
TRIM26
1.000 6 30199158 splice region variant G/A snv 0.12 4
rs9261567 1.000 6 30217467 upstream gene variant T/C snv 0.12 4
rs3130380
HCG18 ; HCG17
0.807 0.280 6 30311353 intron variant G/A snv 6.6E-02 10
rs28780099 1.000 6 30383640 intergenic variant A/G snv 6.4E-02 4
rs17475879 0.925 0.040 6 30396731 regulatory region variant C/T snv 5.6E-02 5
rs28780106 1.000 6 30483738 upstream gene variant G/A snv 6.6E-02 4
rs2524222
GNL1
0.925 0.040 6 30543393 3 prime UTR variant C/T snv 0.16 4
rs2535323 1.000 6 30750403 intron variant A/G snv 0.17 4
rs562932852 1.000 6 30750403 intron variant A/G snv 4
rs17481190
HCG20
1.000 6 30775237 intron variant C/T snv 0.16 4
rs12526481
HCG20
1.000 6 30778856 intron variant C/A snv 0.33 4
rs10947091
HCG20
1.000 6 30779439 intron variant C/G;T snv 4
rs13220225
HCG20
1.000 6 30780025 intron variant G/A snv 0.16 4
rs9468830
HCG20
1.000 6 30781935 non coding transcript exon variant T/G snv 0.36 4
rs12527415
HCG20
1.000 6 30786763 intron variant C/T snv 0.35 4
rs16897900
HCG20
1.000 6 30788116 intron variant C/A snv 0.35 4
rs13201769
HCG20
1.000 6 30788289 intron variant G/A snv 0.35 4
rs4711229
HCG20
1.000 6 30788967 intron variant G/T snv 0.35 4
rs4713367
HCG20
1.000 6 30789045 intron variant G/A snv 0.35 4
rs10947095
HCG20
1.000 6 30789798 intron variant C/T snv 0.35 4
rs11758688
HCG20
1.000 6 30790571 intron variant C/T snv 0.35 4