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: rs17309872
rs17309872
2 0.925 0.080 20 34927985 downstream gene variant A/C;G;T snv 0.700 1.000 1 2010 2010
dbSNP: rs2295097
rs2295097
2 20 34890418 intron variant A/C snv 5.9E-02 0.700 1.000 1 2010 2010