Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs11041816 11 8222251 downstream gene variant A/G snv 0.36 1
rs1120557 14 62662722 regulatory region variant A/G snv 0.88 1
rs12385797 11 106465562 upstream gene variant C/A snv 6.4E-02 1
rs16993414 20 7327891 intergenic variant T/C snv 2.4E-02 1
rs17066694 5 166334297 intergenic variant A/G snv 4.8E-02 1
rs1974620 1.000 0.080 7 15025842 intergenic variant C/A;T snv 1
rs2166706 1.000 0.080 11 92958366 intergenic variant T/A;C snv 1
rs895636 2 44961214 non coding transcript exon variant C/T snv 0.23 1
rs9981885 21 18958319 intron variant A/C snv 0.22 1
rs16856247
ABCB11
2 168927903 intron variant C/T snv 6.6E-02 1
rs853778
ABCB11
2 168954714 intron variant T/C snv 0.53 1
rs6555474
ADCY2
5 7529700 intron variant G/A snv 0.44 1
rs13100723
ARHGEF3
3 56764467 intron variant C/T snv 7.0E-02 1
rs11571943
CDC5L
6 44403953 synonymous variant T/C snv 2.1E-02 2.9E-02 1
rs4682484
CFAP44
3 113304023 missense variant T/A;C snv 0.98 1
rs13427272
CTNNA2
2 80058810 intron variant G/A snv 5.4E-02 1
rs339416
DNAH5
5 13986417 regulatory region variant G/A snv 3.5E-02 1
rs780095
GCKR
2 27518238 intron variant A/G snv 0.60 1
rs7034200
GLIS3
1.000 0.080 9 4289050 intron variant C/A;G snv 1
rs10248619
GRB10
7 50683393 intron variant T/C snv 0.71 1
rs6048205
LINC00261
1.000 0.080 20 22578963 upstream gene variant A/G snv 9.1E-02 1
rs13179048
LOC101929710 ; MIR583HG
5 96207022 intron variant C/A snv 0.23 1
rs6235
LOC101929710 ; PCSK1
0.925 0.120 5 96393194 missense variant C/G snv 0.26 0.23 1
rs234148
LOC105370650
14 97688682 upstream gene variant T/C;G snv 1
rs4841132
LOC157273
8 9326086 non coding transcript exon variant A/G snv 0.89 1