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: rs4770891
rs4770891
1 13 25983588 intron variant C/G snv 8.0E-02 0.700 1.000 1 2018 2018
dbSNP: rs7335338
rs7335338
1 13 25668367 intron variant T/A;C snv 0.700 1.000 1 2018 2018