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: rs7547519
rs7547519
1 1 7256076 intron variant A/G snv 0.76 0.700 1.000 1 2007 2007
dbSNP: rs7594645
rs7594645
1 2 206781950 intron variant A/G snv 7.8E-02 0.700 1.000 1 2015 2015