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: rs9924561
rs9924561
3 16 264781 intron variant G/A;T snv 2.9E-05; 6.5E-03 0.800 1.000 3 2013 2019
dbSNP: rs1122794
rs1122794
2 16 259156 intron variant C/A snv 0.19 0.800 1.000 2 2012 2013
dbSNP: rs13335629
rs13335629
4 16 260381 intron variant G/A;C snv 1.1E-02 0.800 1.000 2 2013 2019
dbSNP: rs13339636
rs13339636
5 16 248589 intron variant A/G snv 3.8E-02 0.800 1.000 2 2013 2017
dbSNP: rs11248914
rs11248914
1 16 243563 intron variant T/C snv 0.36 0.700 1.000 1 2012 2012
dbSNP: rs11248915
rs11248915
1 16 243916 intron variant G/A snv 6.1E-02 0.700 1.000 1 2012 2012
dbSNP: rs13331259
rs13331259
14 16 249924 intron variant A/G snv 3.0E-02 0.700 1.000 1 2019 2019
dbSNP: rs151330263
rs151330263
2 16 252162 intron variant A/G snv 1.0E-02 0.700 1.000 1 2019 2019
dbSNP: rs7189020
rs7189020
2 16 254804 intron variant A/T snv 0.55 0.700 1.000 1 2012 2012
dbSNP: rs76792961
rs76792961
13 16 243594 intron variant C/T snv 7.3E-03 0.700 1.000 1 2019 2019