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: rs2060658
rs2060658
1 11 10312302 intron variant T/C snv 0.50 0.700 1.000 1 2012 2012
dbSNP: rs7944706
rs7944706
1 11 10309764 intron variant G/A snv 0.38 0.700 1.000 1 2012 2012