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: rs121907981
rs121907981
3 0.882 0.120 15 72345550 missense variant C/G snv 1.2E-05 7.0E-06 0.010 1.000 1 1998 1998