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: rs4394274
rs4394274
1 1.000 0.200 6 31350387 intron variant C/A snv 0.40 0.700 1.000 1 2012 2012
dbSNP: rs9368678
rs9368678
1 1.000 0.200 6 31304686 intron variant T/C snv 9.2E-02 0.700 1.000 1 2013 2013