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: rs76904798
rs76904798
2 0.925 0.080 12 40220632 intron variant C/T snv 0.13 0.710 1.000 3 2014 2017
dbSNP: rs11564273
rs11564273
1 1.000 0.040 12 40204350 intron variant T/G snv 6.5E-02 0.700 1.000 1 2012 2012
dbSNP: rs2046932
rs2046932
1 1.000 0.040 12 40186638 intron variant G/A snv 4.8E-02 0.700 1.000 1 2014 2014
dbSNP: rs10878226
rs10878226
1 1.000 0.040 12 40223890 non coding transcript exon variant G/A;C snv 0.010 1.000 1 2012 2012
dbSNP: rs117762348
rs117762348
1 1.000 0.040 12 40203810 non coding transcript exon variant A/G snv 6.5E-02 0.010 1.000 1 2013 2013
dbSNP: rs1491923
rs1491923
1 1.000 0.040 12 40197315 intron variant A/G snv 0.35 0.010 1.000 1 2009 2009