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: rs2066808
rs2066808
8 0.807 0.280 12 56344189 intron variant A/G snv 0.21 0.810 1.000 5 2009 2015
dbSNP: rs2066819
rs2066819
2 0.925 0.040 12 56356420 intron variant C/T snv 4.9E-02 4.5E-02 0.800 1.000 1 2012 2012
dbSNP: rs11575234
rs11575234
1 1.000 0.040 12 56350492 intron variant C/G;T snv 0.700 1.000 1 2015 2015
dbSNP: rs2066807
rs2066807
4 0.925 0.080 12 56346898 missense variant C/G snv 4.9E-02 4.6E-02 0.700 1.000 1 2015 2015