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: rs56238684
rs56238684
4 0.882 0.080 20 34648892 intron variant G/C snv 4.2E-02 0.700 1.000 1 2018 2018
dbSNP: rs910873
rs910873
3 0.882 0.160 20 34583968 intron variant G/A;C snv 0.010 < 0.001 1 2009 2009