Variant Gene N. diseases v DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs121434244
rs121434244
2 1.000 0.200 2 31526225 missense variant G/A snv 2.8E-05 0.800 1.000 24 1977 2016
dbSNP: rs121434245
rs121434245
3 0.882 0.200 2 31580737 missense variant A/T snv 0.800 1.000 16 1992 2005
dbSNP: rs772283403
rs772283403
1 1.000 0.200 2 31526257 missense variant T/A snv 7.0E-06 0.800 1.000 16 1992 2005
dbSNP: rs121913494
rs121913494
7 0.827 0.240 20 58909541 missense variant A/G;T snv 0.010 1.000 1 2019 2019
dbSNP: rs1386577803
rs1386577803
AR
4 0.851 0.240 X 67722872 missense variant G/A snv 0.010 < 0.001 1 2019 2019
dbSNP: rs9332969
rs9332969
AR
5 0.827 0.240 X 67722899 missense variant G/A;T snv 0.010 < 0.001 1 2019 2019
dbSNP: rs1057517829
rs1057517829
1 1.000 0.200 2 31531376 missense variant G/A snv 7.0E-06 0.700 0
dbSNP: rs1200261940
rs1200261940
1 1.000 0.200 2 31531384 stop gained G/A;T snv 0.700 0
dbSNP: rs1331249320
rs1331249320
1 1.000 0.200 2 31533681 missense variant C/T snv 0.700 0
dbSNP: rs1340425455
rs1340425455
1 1.000 0.200 2 31533768 splice acceptor variant T/A;C snv 0.700 0
dbSNP: rs1553323033
rs1553323033
1 1.000 0.200 2 31526232 frameshift variant G/- delins 0.700 0
dbSNP: rs1553323036
rs1553323036
1 1.000 0.200 2 31526236 missense variant T/C snv 0.700 0
dbSNP: rs1553323488
rs1553323488
1 1.000 0.200 2 31529322 missense variant G/A snv 0.700 0
dbSNP: rs1553329427
rs1553329427
4 0.851 0.200 2 31580683 frameshift variant A/- del 0.700 0
dbSNP: rs1553329443
rs1553329443
1 1.000 0.200 2 31580696 missense variant C/A snv 0.700 0
dbSNP: rs587776566
rs587776566
1 1.000 0.200 2 31531448 inframe deletion ATT/- del 0.700 0
dbSNP: rs587776567
rs587776567
1 1.000 0.200 2 31526208 frameshift variant T/- del 0.700 0
dbSNP: rs121434249
rs121434249
4 0.851 0.280 2 31529323 missense variant C/G;T snv 4.0E-06 0.800 1.000 19 1992 2013
dbSNP: rs1351269392
rs1351269392
1 1.000 0.200 2 31580647 missense variant C/T snv 4.7E-06 7.0E-06 0.700 0
dbSNP: rs759561106
rs759561106
1 1.000 0.200 2 31533615 missense variant G/A snv 6.3E-06 2.1E-05 0.700 0
dbSNP: rs761824859
rs761824859
1 1.000 0.200 2 31580842 missense variant A/G snv 8.3E-06 0.700 0
dbSNP: rs1060499834
rs1060499834
1 1.000 0.200 2 31580690 stop gained G/A snv 8.6E-06 0.700 0
dbSNP: rs201175894
rs201175894
1 1.000 0.200 2 31580630 missense variant A/C;G snv 8.1E-05; 1.0E-05 0.700 0
dbSNP: rs767564684
rs767564684
1 1.000 0.200 2 31529385 missense variant G/T snv 1.2E-05 7.0E-06 0.800 1.000 5 1992 2011
dbSNP: rs121434253
rs121434253
1 1.000 0.200 2 31529414 missense variant C/A snv 1.2E-05 0.800 1.000 16 1992 2005