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: rs387906711
rs387906711
6 0.807 0.120 X 56565389 missense variant C/A;T snv 6.6E-06 0.030 1.000 3 2013 2019
dbSNP: rs387906709
rs387906709
9 0.776 0.120 X 56565363 missense variant C/A;T snv 0.020 1.000 2 2019 2019