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: rs9461219
rs9461219
3 0.882 0.160 6 25836699 intron variant C/G;T snv 0.700 1.000 1 2013 2013
dbSNP: rs9467621
rs9467621
2 0.925 0.120 6 25851110 intron variant G/A snv 7.3E-02 0.700 1.000 1 2013 2013
dbSNP: rs9467622
rs9467622
2 0.925 0.120 6 25854416 intron variant C/A;T snv 0.700 1.000 1 2013 2013
dbSNP: rs9467626
rs9467626
4 0.882 0.160 6 25873518 intron variant C/A snv 7.3E-02 0.700 1.000 1 2013 2013
dbSNP: rs972087
rs972087
2 0.925 0.120 6 25872351 intron variant A/G snv 0.12 0.700 1.000 2 2010 2013