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: rs61750639
rs61750639
3 0.882 0.080 1 94007710 missense variant C/T snv 8.0E-06 1.4E-05 0.700 1.000 2 1997 2009