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: rs17271121
rs17271121
4 0.925 0.120 6 25863422 intron variant T/C snv 8.9E-02 0.700 1.000 1 2009 2009
dbSNP: rs3887266
rs3887266
6 0.925 0.120 6 25843518 intron variant C/T snv 8.9E-02 0.700 1.000 1 2009 2009
dbSNP: rs717551
rs717551
2 6 25855396 intron variant T/C snv 0.16 0.700 1.000 1 2009 2009