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: rs61742739
rs61742739
1 1.000 0.160 16 31490477 missense variant A/G snv 5.6E-03 5.2E-03 0.800 1.000 1 2004 2004
dbSNP: rs1309307492
rs1309307492
1 1.000 0.160 16 31489124 missense variant G/A snv 0.700 0
dbSNP: rs387906682
rs387906682
1 1.000 0.160 16 31489034 missense variant C/G snv 0.700 0