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: rs2072803
rs2072803
1 1.000 0.040 6 26392287 missense variant G/C snv 8.6E-02 7.7E-02 0.700 1.000 1 2009 2009
dbSNP: rs2072806
rs2072806
1 1.000 0.040 6 26384865 intron variant C/G snv 7.7E-02 0.700 1.000 1 2009 2009