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: rs1352015
rs1352015
1 1.000 0.080 X 66624001 intron variant G/A snv 0.700 1.000 1 2012 2012
dbSNP: rs1385699
rs1385699
1 1.000 0.080 X 66605144 missense variant C/T snv 0.79 0.61 0.700 1.000 1 2012 2012
dbSNP: rs4827379
rs4827379
1 1.000 0.080 X 66594118 downstream gene variant T/C snv 0.700 1.000 1 2012 2012