Source: CURATED

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs137852596
AR
1.000 0.160 X 67643371 missense variant G/A snv 1
rs137852597
AR
1.000 0.160 X 67722973 missense variant T/C snv 1
rs137852598
AR
1.000 0.160 X 67722948 missense variant C/G;T snv 5.5E-06 1
rs137852599
AR
1.000 0.160 X 67711585 missense variant A/C snv 1
rs139524801
AR
0.925 0.160 X 67643283 missense variant G/A;T snv 1.8E-04 1
rs1481151440
AR
1.000 0.160 X 67545467 stop gained C/A;T snv 1
rs1555969512
AR
1.000 0.160 X 67545360 stop gained C/T snv 1
rs1555969545
AR
1.000 0.160 X 67545414 stop gained C/T snv 1
rs1555969682
AR
1.000 0.160 X 67545889 missense variant G/T snv 1
rs1555969694
AR
1.000 0.160 X 67545936 frameshift variant -/G delins 1
rs1555969807
AR
1.000 0.160 X 67546331 stop gained C/A snv 1
rs1555982860
AR
1.000 0.160 X 67643327 missense variant G/A snv 1
rs1555990485
AR
1.000 0.160 X 67686087 missense variant C/T snv 1
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
rs1555995816
AR
1.000 0.160 X 67711560 missense variant G/A 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
rs1555995865
AR
1.000 0.160 X 67711671 missense variant T/C snv 1
rs1555995877
AR
1.000 0.160 X 67711687 missense variant C/T snv 1
rs1555996855
AR
1.000 0.160 X 67717570 frameshift variant A/- del 1
rs1555996867
AR
1.000 0.160 X 67717603 missense variant C/G snv 1
rs1555997625
AR
1.000 0.160 X 67721951 missense variant C/T snv 1