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: rs7203560
rs7203560
7 1.000 0.080 16 134391 intron variant T/G snv 2.0E-02 0.800 1.000 2 2013 2017
dbSNP: rs117747069
rs117747069
4 16 120077 intron variant G/C snv 2.5E-02 0.700 1.000 2 2016 2016
dbSNP: rs11248850
rs11248850
2 16 113599 intron variant G/A snv 0.38 0.700 1.000 1 2012 2012
dbSNP: rs2238368
rs2238368
4 16 120329 intron variant C/T snv 0.36 0.700 1.000 1 2016 2016
dbSNP: rs545105162
rs545105162
1 16 98445 intron variant G/A snv 5.4E-04 0.700 1.000 1 2016 2016
dbSNP: rs6600233
rs6600233
3 16 93505 intron variant C/G;T snv 0.700 1.000 1 2018 2018
dbSNP: rs8055187
rs8055187
1 16 108326 intron variant A/T snv 0.37 0.700 1.000 1 2019 2019