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: rs17868320
rs17868320
1 2 233669782 intron variant C/T snv 4.0E-02 0.010 1.000 1 2012 2012
dbSNP: rs4124874
rs4124874
8 0.851 0.120 2 233757013 intron variant T/A;G snv 0.010 1.000 1 2017 2017