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: rs1805034
rs1805034
12 0.742 0.360 18 62360008 missense variant C/T snv 0.54 0.56 0.010 1.000 1 2012 2012
dbSNP: rs35211496
rs35211496
5 0.851 0.200 18 62354528 missense variant C/T snv 0.12 0.12 0.010 1.000 1 2012 2012