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: rs695871
rs695871
2 1.000 0.080 12 111599196 missense variant G/C snv 0.77 0.61 0.010 1.000 1 2011 2011
dbSNP: rs695872
rs695872
2 0.925 0.120 12 111599125 synonymous variant G/A snv 0.79 0.61 0.010 1.000 1 2011 2011