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: rs58862095
rs58862095
1 7 75452145 intron variant C/G;T snv 0.700 1.000 1 2019 2019
dbSNP: rs6944634
rs6944634
1 7 75432493 intron variant G/A;C snv 0.700 1.000 1 2019 2019