Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs886041065
ASXL2
0.677 0.600 2 25743913 frameshift variant G/- delins 43
rs1014959895
PRMT7
0.763 0.360 16 68329105 stop gained G/C;T snv 4.0E-06; 1.6E-05 16
rs1251713297
PRMT7
0.776 0.360 16 68355785 stop gained C/A snv 8.1E-06 15
rs17254590 13 106384996 downstream gene variant G/C snv 2.8E-02 2
rs62519907 8 71696834 intron variant G/A;T snv 0.17 2
rs77164426 2 146756888 intergenic variant A/G snv 1.8E-02 2
rs113847670
DOCK1
10 127076415 intron variant C/T snv 3.3E-02 2
rs121913139
INSR
1.000 0.120 19 7122662 missense variant C/T snv 2
rs10829848 10 130949624 intergenic variant C/T snv 0.15 1
rs11682922 2 7654805 intergenic variant G/T snv 0.52 1
rs12655917 5 77996116 downstream gene variant G/A snv 4.2E-02 1
rs17431357 12 120442631 intron variant C/T snv 4.5E-02 1
rs4427876 18 39171334 intergenic variant C/T snv 0.75 1
rs7077836 10 130953235 intergenic variant G/A snv 0.15 1
rs8093427 18 39191160 intergenic variant T/A;C snv 1
rs9396607 6 15855197 intergenic variant G/T snv 2.6E-02 1
rs9524298
GPC6
13 93980567 intron variant G/A snv 0.17 1
rs121913157
INSR
19 7120739 missense variant C/T snv 1
rs1568426700
INSR
19 7120678 missense variant G/A snv 1
rs6576507
LINC02346
15 26043247 intron variant T/C snv 4.5E-02 1
rs10512148
LOC102724036
9 84494571 intron variant A/C;G snv 1
rs1077625
LOC102724036
9 84519729 intron variant A/G snv 3.5E-02 1
rs13295359
LOC102724036
9 84558757 intron variant C/T snv 3.4E-02 1
rs13295556
LOC102724036
9 84493940 intron variant C/T snv 4.2E-02 1
rs13297129
LOC102724036
9 84494136 intron variant T/C snv 4.1E-02 1