Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1260333 0.882 0.160 2 27525757 downstream gene variant A/G snv 0.58 12
rs2911711 0.925 0.120 2 27527679 downstream gene variant T/A snv 0.58 6
rs11667159 19 46291989 intergenic variant C/A;T snv 3
rs11668290 19 46292921 upstream gene variant G/A snv 0.12 3
rs11671319 19 46291810 intergenic variant T/C snv 0.12 3
rs11671360 19 46291914 intergenic variant T/C snv 0.12 3
rs11671710 19 46288677 regulatory region variant C/G;T snv 3
rs117366905 19 46294033 upstream gene variant A/G snv 0.12 3
rs117992292 19 46294038 upstream gene variant A/G snv 0.12 3
rs141332218 19 46293976 upstream gene variant T/C snv 0.12 3
rs142815467 19 46291277 intergenic variant -/T delins 0.12 3
rs174448 1.000 0.120 11 61872101 downstream gene variant G/A snv 0.61 3
rs34128150 19 46291852 intergenic variant C/A snv 0.12 3
rs7254961 19 46292627 upstream gene variant C/T snv 0.12 3
rs7256047 19 46292776 upstream gene variant T/C snv 0.12 3
rs73059722 19 46293161 upstream gene variant G/A snv 0.12 3
rs73059723 19 46293245 upstream gene variant A/C snv 0.12 3
rs73059724 19 46293510 upstream gene variant T/C snv 0.11 3
rs73059725 19 46293511 upstream gene variant G/A snv 0.11 3
rs73059726 19 46293937 upstream gene variant G/A snv 0.12 3
rs80095739 19 46282441 regulatory region variant A/G snv 0.10 3
rs10414689 19 51293045 regulatory region variant T/C snv 0.11 2
rs10517480 4 59883111 intergenic variant A/T snv 0.27 2
rs11230815 11 61868654 downstream gene variant G/C;T snv 2
rs12529874 6 98014625 intron variant G/A snv 2.6E-02 2