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: rs756151230
rs756151230
1 1.000 7 92470377 missense variant G/C snv 0.010 1.000 1 2001 2001