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: rs1057519780
rs1057519780
1 1.000 0.120 1 11127800 missense variant C/T snv 0.700 1.000 1 2014 2014
dbSNP: rs587777900
rs587777900
1 1.000 0.120 1 11114363 missense variant C/T snv 0.700 1.000 1 2014 2014