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: rs28900396
rs28900396
3 2 233761914 intron variant T/C snv 6.4E-02 0.700 1.000 1 2012 2012
dbSNP: rs28900402
rs28900402
1 2 233767766 intron variant C/T snv 2.7E-02 0.700 1.000 1 2012 2012