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: rs415929
rs415929
2 0.925 0.200 6 32221255 synonymous variant T/C snv 0.31 0.29 0.700 1.000 1 2009 2009
dbSNP: rs8192590
rs8192590
1 1.000 0.080 6 32220006 intron variant C/G snv 1.9E-02 0.700 1.000 1 2009 2009