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: rs4929949
rs4929949
4 1.000 0.080 11 8583046 intron variant T/C snv 0.46 0.700 1.000 2 2010 2013
dbSNP: rs10769908
rs10769908
4 11 8462542 intron variant C/T snv 0.55 0.700 1.000 1 2009 2009