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: rs56984562
rs56984562
6 0.827 0.200 1 156137666 missense variant C/A;G;T snv 0.010 1.000 1 2010 2010
dbSNP: rs59301204
rs59301204
4 0.925 0.080 1 156135956 missense variant G/A;C snv 1.2E-05 0.010 1.000 1 2017 2017