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: rs1545
rs1545
2 0.925 0.080 20 10405365 missense variant C/A snv 0.14 0.14 0.010 1.000 1 2008 2008
dbSNP: rs1547
rs1547
2 0.925 0.080 20 10405411 missense variant G/A snv 0.14 0.14 0.010 1.000 1 2005 2005
dbSNP: rs74315394
rs74315394
4 0.851 0.440 20 10412791 missense variant C/A snv 5.2E-03 5.0E-03 0.010 1.000 1 2005 2005