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: rs369487110
rs369487110
1 1.000 0.080 1 36098770 missense variant C/G;T snv 4.1E-06; 1.1E-04 4.9E-05 0.700 1.000 1 2001 2001