Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs964184
ZPR1
0.716 0.440 11 116778201 3 prime UTR variant G/C snv 0.82 47
rs115849089 8 20054859 intergenic variant G/A snv 9.8E-02 7
rs150641967
HAPLN4
19 19259532 intron variant AGAC/-;AGACAGAC delins 4
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
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
rs145556679
DSCAML1
11 117772549 intron variant G/A;C snv 2
rs3826796
HIF3A
19 46296578 upstream gene variant G/T snv 7.7E-02 2