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: rs1057516085
rs1057516085
8 0.827 0.080 20 63444747 missense variant C/T snv 0.010 1.000 1 2017 2017
dbSNP: rs1057518443
rs1057518443
3 1.000 0.040 X 120557964 missense variant T/C snv 0.010 1.000 1 2018 2018
dbSNP: rs1057524792
rs1057524792
3 1.000 0.040 4 39467617 missense variant T/G snv 0.010 1.000 1 2018 2018
dbSNP: rs751866383
rs751866383
3 1.000 0.040 4 39470047 missense variant G/T snv 4.0E-06 0.010 1.000 1 2018 2018
dbSNP: rs771844443
rs771844443
3 1.000 0.040 2 165309194 missense variant A/G snv 4.0E-06 0.010 1.000 1 2018 2018
dbSNP: rs796052650
rs796052650
4 0.925 0.040 20 63413574 missense variant G/A;C snv 0.010 1.000 1 2018 2018
dbSNP: rs796053150
rs796053150
3 1.000 0.040 2 165386827 missense variant A/G snv 0.010 1.000 1 2018 2018
dbSNP: rs866291718
rs866291718
3 1.000 0.040 4 39470042 missense variant A/G snv 0.010 1.000 1 2018 2018
dbSNP: rs886041715
rs886041715
7 0.827 0.040 16 56192353 missense variant G/A;C;T snv 0.010 1.000 1 2018 2018
dbSNP: rs961150638
rs961150638
3 1.000 0.040 4 39470038 missense variant G/C snv 4.0E-06 0.010 1.000 1 2018 2018