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: rs10035432
rs10035432
1 1.000 0.040 5 147855193 upstream gene variant G/A snv 0.18 0.010 1.000 1 2015 2015
dbSNP: rs10054105
rs10054105
3 0.925 0.080 5 111573636 intron variant T/G snv 0.17 0.700 1.000 1 2018 2018
dbSNP: rs1024611
rs1024611
63 0.568 0.800 17 34252769 upstream gene variant A/G snv 0.28 0.010 1.000 1 2019 2019
dbSNP: rs103294
rs103294
7 0.827 0.200 19 54293995 downstream gene variant T/C snv 0.82 0.010 1.000 1 2013 2013
dbSNP: rs10459953
rs10459953
3 0.925 0.080 17 27800492 5 prime UTR variant C/A;G;T snv 0.010 1.000 1 2010 2010
dbSNP: rs1057519912
rs1057519912
11 0.776 0.200 X 71129408 missense variant C/G;T snv 0.010 1.000 1 2016 2016
dbSNP: rs10786938
rs10786938
1 1.000 0.040 10 106280012 intergenic variant G/C;T snv 0.700 1.000 1 2019 2019
dbSNP: rs10983755
rs10983755
7 0.790 0.320 9 117702392 upstream gene variant G/A snv 3.2E-02 0.010 1.000 1 2019 2019
dbSNP: rs11084596
rs11084596
3 1.000 0.040 19 31614073 regulatory region variant T/C snv 0.35 0.700 1.000 1 2018 2018
dbSNP: rs11199879
rs11199879
3 1.000 0.040 10 121285698 regulatory region variant T/C snv 0.18 0.700 1.000 1 2018 2018
dbSNP: rs1126647
rs1126647
8 0.827 0.160 4 73743328 3 prime UTR variant A/T snv 0.31 0.010 1.000 1 2019 2019
dbSNP: rs115336889
rs115336889
1 1.000 0.040 5 10454257 intron variant G/A;C snv 0.010 1.000 1 2019 2019
dbSNP: rs11651052
rs11651052
7 0.851 0.200 17 37742390 intron variant G/A snv 0.50 0.700 1.000 1 2018 2018
dbSNP: rs12470143
rs12470143
2 0.925 0.080 2 31538488 intron variant C/T snv 0.42 0.010 1.000 1 2017 2017
dbSNP: rs12621278
rs12621278
7 0.790 0.280 2 172446825 intron variant A/G snv 4.9E-02 0.010 1.000 1 2013 2013
dbSNP: rs12653946
rs12653946
5 0.882 0.080 5 1895715 intron variant C/T snv 0.43 0.010 1.000 1 2013 2013
dbSNP: rs12826786
rs12826786
26 0.683 0.480 12 53961717 upstream gene variant C/T snv 0.38 0.010 1.000 1 2017 2017
dbSNP: rs137852569
rs137852569
AR
10 0.752 0.320 X 67686030 missense variant G/A snv 9.4E-06 0.010 1.000 1 2005 2005
dbSNP: rs141179786
rs141179786
1 1.000 0.040 18 53662174 intergenic variant A/G;T snv 2.2E-02 0.700 1.000 1 2019 2019
dbSNP: rs148678804
rs148678804
2 1.000 0.040 10 22138360 intergenic variant G/A;T snv 0.700 1.000 1 2018 2018
dbSNP: rs1638703
rs1638703
2 1.000 0.040 13 50514220 intron variant G/C snv 0.27 0.700 1.000 1 2018 2018
dbSNP: rs16902947
rs16902947
1 1.000 0.040 5 36308995 intergenic variant A/G snv 0.22 0.010 1.000 1 2017 2017
dbSNP: rs17144046
rs17144046
4 0.882 0.120 10 8564051 intergenic variant A/G snv 0.28 0.700 1.000 1 2017 2017
dbSNP: rs1800795
rs1800795
140 0.494 0.840 7 22727026 intron variant C/G snv 0.71 0.010 1.000 1 2019 2019
dbSNP: rs1899663
rs1899663
22 0.683 0.280 12 53967210 intron variant C/A snv 0.28 0.010 1.000 1 2017 2017