Source: CURATED

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs139524801
AR
0.925 0.160 X 67643283 missense variant G/A;T snv 1.8E-04 1
rs137852588
AR
0.925 0.160 X 67643284 missense variant C/T snv 2
rs886041050
AR
1.000 0.160 X 67643324 missense variant T/C snv 1
rs1555982860
AR
1.000 0.160 X 67643327 missense variant G/A snv 1
rs137852596
AR
1.000 0.160 X 67643371 missense variant G/A snv 1
rs137852586
AR
1.000 0.160 X 67643378 missense variant G/A;T snv 1
rs137852587
AR
0.925 0.160 X 67643387 missense variant T/A snv 2
rs1555982894
AR
0.925 0.160 X 67643409 splice donor variant T/C snv 2
rs137852566
AR
1.000 0.160 X 67686012 stop gained A/T snv 1
rs137852569
AR
0.752 0.320 X 67686030 missense variant G/A snv 9.4E-06 3
rs1555990470
AR
0.925 0.200 X 67686046 missense variant G/A snv 2
rs137852573
AR
0.807 0.280 X 67686064 missense variant G/A snv 4
rs1555990485
AR
1.000 0.160 X 67686087 missense variant C/T snv 1
rs754201976
AR
0.925 0.160 X 67686088 missense variant G/A snv 5.5E-06 2
rs1555990488
AR
1.000 0.160 X 67686091 missense variant T/C snv 1
rs1555995750
AR
1.000 0.160 X 67711402 frameshift variant C/- delins 1
rs137852579
AR
1.000 0.160 X 67711549 missense variant T/C snv 1
rs1555995816
AR
1.000 0.160 X 67711560 missense variant G/A snv 1
rs1555995822
AR
0.925 0.200 X 67711569 missense variant G/A snv 2
rs137852599
AR
1.000 0.160 X 67711585 missense variant A/C snv 1
rs1555995840
AR
1.000 0.160 X 67711602 missense variant G/A snv 1
rs1555995842
AR
1.000 0.160 X 67711606 missense variant C/A snv 1
rs1555995848
AR
1.000 0.160 X 67711619 missense variant G/T snv 1
rs1555995851
AR
1.000 0.160 X 67711620 missense variant C/T snv 1
rs864622007
AR
0.882 0.200 X 67711621 missense variant T/A snv 2