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: rs1122794
rs1122794
2 16 259156 intron variant C/A snv 0.19 0.800 1.000 2 2009 2017
dbSNP: rs13331259
rs13331259
14 16 249924 intron variant A/G snv 3.0E-02 0.700 1.000 2 2019 2019
dbSNP: rs9924561
rs9924561
3 16 264781 intron variant G/A;T snv 2.9E-05; 6.5E-03 0.700 1.000 2 2013 2017
dbSNP: rs13339636
rs13339636
5 16 248589 intron variant A/G snv 3.8E-02 0.700 1.000 1 2013 2013
dbSNP: rs3743879
rs3743879
2 16 268475 3 prime UTR variant C/A;G snv 0.700 1.000 1 2019 2019