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: rs1898671
rs1898671
5 0.851 0.160 5 111072304 intron variant C/T snv 0.25 0.010 1.000 1 2019 2019
dbSNP: rs2289278
rs2289278
5 0.827 0.200 5 111073450 5 prime UTR variant C/G snv 8.7E-02 0.010 1.000 1 2016 2016