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: rs202247756
rs202247756
2 1.000 0.080 10 102550019 missense variant C/T snv 0.010 1.000 1 2012 2012