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: rs1057519946
rs1057519946
9 0.784 0.179 19 52212729 missense variant C/G,T snp 0.700 1 2016 2016
dbSNP: rs1057519947
rs1057519947
9 0.784 0.179 19 52212730 missense variant G/A snp 0.700 1 2016 2016
dbSNP: rs786205228
rs786205228
3 0.878 0.071 19 52212718 missense variant C/G,T snp 0.700 1 2016 2016