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: rs1064794292
rs1064794292
3 0.882 0.200 9 21974760 missense variant C/T snv 0.700 0
dbSNP: rs121913385
rs121913385
9 0.763 0.240 9 21971112 missense variant G/A;C snv 0.700 0
dbSNP: rs1444669684
rs1444669684
36 0.658 0.480 9 21994285 missense variant C/A;T snv 0.030 1.000 3 2007 2016