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: rs1064794259
rs1064794259
2 1.000 0.080 19 11113615 missense variant C/T snv 0.010 1.000 1 2008 2008
dbSNP: rs770696696
rs770696696
2 1.000 0.080 19 11113738 missense variant C/T snv 4.0E-06 0.010 1.000 1 2008 2008