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: rs1419539530
rs1419539530
1 1.000 0.080 21 40189232 missense variant G/A snv 9.5E-06 7.0E-06 0.700 0
dbSNP: rs2837770
rs2837770
1 1.000 0.080 21 40662426 intron variant G/A snv 0.34 0.010 1.000 1 2018 2018