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: rs17646665
rs17646665
4 1.000 0.080 1 109369429 intron variant A/G snv 5.8E-02 0.700 1.000 1 2012 2012
dbSNP: rs17646731
rs17646731
3 1 109376903 intron variant G/A snv 4.6E-02 0.700 1.000 1 2012 2012
dbSNP: rs4970843
rs4970843
3 1 109344569 intron variant T/C snv 0.37 0.700 1.000 1 2012 2012