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: rs16942333
rs16942333
3 15 88845033 intron variant A/G snv 3.3E-02 0.700 1.000 1 2012 2012
dbSNP: rs8026235
rs8026235
1 15 88806225 intron variant A/C snv 1.7E-02 0.700 1.000 1 2012 2012