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: rs12632583
rs12632583
1 1.000 0.040 3 169464399 intron variant A/G snv 4.1E-02 0.700 1.000 1 2017 2017
dbSNP: rs1918976
rs1918976
1 1.000 0.040 3 169466635 intron variant C/T snv 1.5E-02 0.700 1.000 1 2017 2017
dbSNP: rs3817581
rs3817581
1 1.000 0.040 3 169463794 intron variant C/T snv 0.45 0.700 1.000 1 2017 2017
dbSNP: rs4955659
rs4955659
1 1.000 0.040 3 169453830 intron variant A/T snv 4.1E-02 0.700 1.000 1 2017 2017
dbSNP: rs556915505
rs556915505
5 0.851 0.080 3 169143780 missense variant T/C snv 4.0E-06 7.0E-06 0.010 1.000 1 2011 2011
dbSNP: rs751689316
rs751689316
4 0.925 0.080 3 169131510 missense variant C/T snv 1.2E-05 0.010 1.000 1 2008 2008