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: rs9967792
rs9967792
1 1.000 0.080 2 191109709 intron variant T/C snv 0.65 0.700 1.000 1 2013 2013