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: rs1433722257
rs1433722257
1 1.000 0.120 3 70972170 missense variant C/A;T snv 1.6E-05; 8.1E-06 0.010 1.000 1 2017 2017
dbSNP: rs761606953
rs761606953
1 1.000 0.120 3 70972053 missense variant C/T snv 2.8E-05 0.010 1.000 1 2017 2017
dbSNP: rs797045586
rs797045586
3 0.925 0.120 3 70972666 missense variant C/T snv 0.010 1.000 1 2017 2017