Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
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
rs143399767 9 93420421 downstream gene variant A/C snv 6.9E-03 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
rs17407594 1 65704679 intron variant G/A;T snv 1
rs3847554 11 92935660 upstream gene variant C/T snv 0.56 1
rs4836906 9 122665528 downstream gene variant T/C snv 1.6E-02 1
rs533883198 10 3286126 intergenic variant G/A snv 2.1E-03 1
rs7077606 10 53647331 intergenic variant C/T snv 0.15 1
rs7801534 7 49290084 intergenic variant A/G snv 9.6E-02 1
rs7821492 8 76910847 intron variant G/A;C;T snv 1
rs9981885 21 18958319 intron variant A/C snv 0.22 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
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
rs12280680
CREB3L1
11 46279171 intron variant G/A;C snv 1
rs13427272
CTNNA2
2 80058810 intron variant G/A snv 5.4E-02 1
rs10276674
DGKB
7 14882382 intron variant T/C;G snv 1
rs118084662
DHRS7B
17 21169976 intron variant A/G snv 3.3E-04 1
rs339416
DNAH5
5 13986417 regulatory region variant G/A snv 3.5E-02 1
rs455489
DSCAM
21 40567642 intron variant A/C snv 0.15 1
rs540671238
HDAC9
7 18732931 intron variant A/G;T snv 1
rs10815355
KANK1
9 622523 intron variant G/T snv 6.0E-02 1