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: rs1137101
rs1137101
77 0.554 0.760 1 65592830 missense variant A/G snv 0.51 0.50 0.010 1.000 1 2014 2014
dbSNP: rs2234693
rs2234693
77 0.555 0.680 6 151842200 intron variant T/C snv 0.47 0.010 1.000 1 2014 2014
dbSNP: rs2414096
rs2414096
3 0.882 0.240 15 51237582 intron variant G/A snv 0.40 0.010 1.000 1 2014 2014
dbSNP: rs372903533
rs372903533
AR
2 0.925 0.200 X 67711599 missense variant C/T snv 5.5E-06 9.5E-06 0.010 1.000 1 2014 2014
dbSNP: rs3808350
rs3808350
6 0.882 0.080 7 1086257 intron variant A/G;T snv 0.010 1.000 1 2015 2015
dbSNP: rs3808351
rs3808351
7 0.827 0.240 7 1087023 5 prime UTR variant G/A snv 0.29 0.010 1.000 1 2015 2015
dbSNP: rs4986938
rs4986938
35 0.641 0.600 14 64233098 3 prime UTR variant C/T snv 0.31 0.33 0.010 1.000 1 2014 2014
dbSNP: rs7799039
rs7799039
33 0.649 0.560 7 128238730 upstream gene variant G/A;C snv 0.010 1.000 1 2014 2014