Source: CURATED ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs13107325
SLC39A8
0.776 0.520 4 102267552 missense variant C/A;T snv 4.0E-06; 4.5E-02 30
rs687621
ABO
0.851 0.240 9 133261662 intron variant G/A;C snv 17
rs6570507
ADGRG6
0.827 0.240 6 142358435 intron variant G/A snv 0.47 11
rs1800469
B9D2 ; TGFB1
0.547 0.760 19 41354391 intron variant A/G snv 0.69 10
rs10830963
MTNR1B
0.776 0.400 11 92975544 intron variant C/G snv 0.22 10
rs137852564
AR
0.827 0.240 X 67722976 missense variant G/A;T snv 5
rs995030
KITLG
0.776 0.320 12 88496894 3 prime UTR variant A/G snv 0.67 5
rs11190870 0.827 0.200 10 101219450 intergenic variant T/A;C snv 4
rs137852573
AR
0.807 0.280 X 67686064 missense variant G/A snv 4
rs2900333
ATF7IP
0.882 0.200 12 14500933 3 prime UTR variant C/A;G;T snv 4
rs662
PON1
0.485 0.840 7 95308134 missense variant T/C snv 0.38 0.42 4
rs12946942 0.882 0.200 17 71240857 intergenic variant G/T snv 7.5E-02 3
rs6137473 0.827 0.280 20 21904055 intergenic variant G/A snv 0.61 3
rs137852569
AR
0.752 0.320 X 67686030 missense variant G/A snv 9.4E-06 3
rs137852577
AR
0.882 0.200 X 67722898 missense variant C/T snv 3
rs137852591
AR
0.851 0.200 X 67721909 missense variant C/G snv 1.4E-03 1.4E-03 3
rs143040492
AR
0.882 0.200 X 67723690 missense variant C/T snv 1.1E-05 9.6E-06 3
rs886041133
AR
0.882 0.200 X 67723746 missense variant G/A;C snv 5.5E-06 3
rs9332969
AR
0.827 0.240 X 67722899 missense variant G/A;T snv 3
rs9332971
AR
0.851 0.200 X 67722944 missense variant G/A;T snv 3
rs10510181
CHL1-AS2
0.882 0.200 3 149364 intron variant G/A snv 0.31 3
rs678741
LBX1-AS1
0.851 0.200 10 101237824 intron variant G/A snv 0.51 3
rs951366
NUCKS1
0.925 0.240 1 205716224 3 prime UTR variant T/C snv 0.34 3
rs11598564 0.925 0.200 10 101204847 intergenic variant G/A snv 0.45 2
rs4794665 1.000 0.160 17 56772968 intergenic variant A/C;G snv 2