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: rs3918226
rs3918226
12 0.925 0.080 7 150993088 intron variant C/T snv 5.7E-02 0.700 1.000 4 2017 2018
dbSNP: rs891511
rs891511
4 7 151007755 intron variant G/A;C snv 0.700 1.000 2 2016 2019