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: rs267606983
rs267606983
2 0.925 0.080 14 73192744 missense variant G/C snv 0.700 0
dbSNP: rs63750886
rs63750886
5 0.851 0.080 14 73198072 missense variant C/G snv 0.700 0