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: rs10810632
rs10810632
1 1.000 0.120 9 16789026 intron variant C/T snv 0.85 0.700 1.000 1 2010 2010