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: rs35210477
rs35210477
2 7 56044524 intron variant A/G snv 4.1E-02 0.700 1.000 1 2019 2019
dbSNP: rs4947534
rs4947534
2 7 56011401 3 prime UTR variant T/A;C snv 0.700 1.000 1 2015 2015
dbSNP: rs7793921
rs7793921
3 7 56053188 intron variant G/A snv 0.64 0.700 1.000 1 2019 2019