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: rs13196377
rs13196377
1 1.000 0.040 6 111580635 intron variant G/A;T snv 0.010 1.000 1 2014 2014
dbSNP: rs7769061
rs7769061
1 1.000 0.040 6 111605706 intron variant A/G snv 7.2E-02 0.700 1.000 1 2015 2015
dbSNP: rs33980500
rs33980500
14 0.742 0.200 6 111592059 missense variant C/T snv 8.6E-02 9.7E-02 0.850 1.000 7 2010 2019
dbSNP: rs13210247
rs13210247
3 0.882 0.280 6 111601517 non coding transcript exon variant A/G snv 0.10 0.700 1.000 1 2010 2010