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: rs12603332
rs12603332
7 0.807 0.200 17 39926554 5 prime UTR variant T/C snv 0.49 0.730 1.000 4 2008 2017
dbSNP: rs8076131
rs8076131
11 0.790 0.200 17 39924659 intron variant G/A;C snv 0.730 1.000 4 2011 2018
dbSNP: rs4795403
rs4795403
1 1.000 0.080 17 39929469 non coding transcript exon variant T/C;G snv 0.700 1.000 1 2011 2011
dbSNP: rs4378650
rs4378650
1 1.000 0.080 17 39924612 intron variant A/G;T snv 0.020 1.000 2 2008 2009
dbSNP: rs3169572
rs3169572
1 1.000 0.080 17 39921159 3 prime UTR variant G/A snv 2.7E-02 0.010 1.000 1 2011 2011
dbSNP: rs4065275
rs4065275
6 0.807 0.160 17 39924612 intron variant A/G;T snv 0.56 0.010 1.000 1 2012 2012
dbSNP: rs4795404
rs4795404
1 1.000 0.080 17 39929538 intron variant A/C;T snv 0.76 0.010 1.000 1 2012 2012