Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs11067773 12 115790690 intron variant T/C snv 7.8E-02 1
rs111724808 1 22411453 intergenic variant T/G snv 3.1E-02 1
rs115545556 5 132143804 downstream gene variant C/T snv 4.4E-03 1
rs115744676 7 94432092 downstream gene variant G/T snv 6.4E-03 1
rs116755262 6 44487396 intergenic variant A/G snv 2.1E-02 1
rs11708896 3 7795937 intergenic variant A/G;T snv 1
rs11763856 7 35506177 intron variant C/T snv 1.9E-02 1
rs12359272 10 95605406 downstream gene variant G/A snv 0.25 1
rs13018106 2 163518692 intergenic variant G/C snv 0.43 1
rs1896312 12 114908619 intergenic variant C/T snv 0.71 1
rs191392302 17 41797709 downstream gene variant T/G snv 3.5E-02 1
rs6489953 12 114326957 intergenic variant C/A;T snv 1
rs6505987 18 1977712 intron variant G/A;T snv 1
rs652673 11 76220247 upstream gene variant C/A;T snv 1
rs6599232 3 38658269 regulatory region variant C/T snv 0.74 1
rs73963343 18 67032737 intergenic variant C/T snv 3.9E-02 1
rs7538988 1 51351869 downstream gene variant T/C snv 2.2E-02 1
rs76270203 12 113499191 intergenic variant A/C snv 2.5E-02 1
rs77202753 5 9619752 downstream gene variant C/T snv 8.3E-03 1
rs79076257 8 109232394 intergenic variant T/C snv 4.3E-02 1
rs8134605 21 30931947 intergenic variant G/A;C snv 1
rs881301 8 38474800 intergenic variant T/A;C snv 1
rs904974 15 70155243 intergenic variant T/C snv 0.87 1
rs9826413 3 27793256 upstream gene variant A/T snv 0.10 1
rs73276602
ABCB5
7 20642227 intron variant A/C;G snv 1