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: rs121908245
rs121908245
1 1.000 0.080 19 13332911 missense variant C/T snv 8.1E-06 7.0E-06 0.700 1.000 6 1997 2017