Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs112827279
LOC102724092
X 15234130 downstream gene variant C/A snv 4.1E-02 2
rs113288656
PTCHD1-AS
X 22417389 intron variant T/C snv 2.1E-02 2
rs12854631 X 58297412 intergenic variant A/C snv 2.7E-02 2
rs137986605 X 134944139 regulatory region variant G/A snv 2.0E-02 2
rs139306621
LOC107985670
X 78678436 intergenic variant C/A;T snv 2
rs139545172 X 19186106 intergenic variant G/A snv 3.7E-02 2
rs139618469 X 143165510 intergenic variant T/C snv 1.4E-02 2
rs140386998 X 100959983 downstream gene variant C/T snv 3.7E-02 2
rs143011308 X 4117086 intergenic variant T/A snv 2.8E-02 2
rs143049324
REPS2
X 17027288 intron variant A/G snv 4.4E-02 2
rs146414513 X 91548679 intergenic variant T/C snv 5.3E-02 2
rs146514374 X 7839126 upstream gene variant G/C snv 2.6E-02 2
rs147428850 X 79047973 intergenic variant G/A snv 2.7E-02 2
rs148215758
PHF8
X 54017674 synonymous variant A/C;T snv 2.6E-02 2
rs149432766 X 93801889 intergenic variant G/A;T snv 2
rs150798856 X 23322339 intergenic variant T/C snv 1.5E-02 2
rs17219051 X 4330060 intergenic variant C/T snv 4.3E-02 2
rs181869920 X 79674625 intergenic variant G/T snv 1.5E-02 2
rs183056377
KLF8
X 56034817 intron variant G/A snv 5.7E-02 2
rs191209518
NHSL2
X 72109657 intron variant C/G;T snv 2
rs191792526 X 44070843 intergenic variant G/A snv 4.7E-03 2
rs191870197
MIR325HG
X 76826573 intron variant C/A snv 3.1E-02 2
rs192657641 X 76601629 intergenic variant C/T snv 2
rs4644421 X 77090709 intergenic variant C/A snv 3.3E-02 2
rs5912268 X 79276916 intergenic variant C/A;G;T snv 2