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: rs9906298
rs9906298
2 0.925 0.040 17 51702890 intron variant T/C snv 9.2E-02 0.700 1.000 1 2007 2007