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: rs1143679
rs1143679
14 0.732 0.520 16 31265490 missense variant G/A snv 9.7E-02 0.11 0.900 1.000 23 2009 2019
dbSNP: rs9888739
rs9888739
3 0.882 0.120 16 31301932 intron variant C/T snv 0.26 0.810 1.000 5 2008 2014
dbSNP: rs1143678
rs1143678
1 1.000 0.080 16 31331684 missense variant C/T snv 0.15 0.17 0.730 1.000 6 2008 2017
dbSNP: rs1143683
rs1143683
1 1.000 0.080 16 31325567 missense variant C/T snv 0.16 0.16 0.730 1.000 4 2009 2013
dbSNP: rs9937837
rs9937837
1 1.000 0.080 16 31287618 intron variant T/G snv 0.40 0.710 1.000 2 2011 2011
dbSNP: rs11860650
rs11860650
3 0.882 0.120 16 31315385 intron variant C/T snv 0.14 0.700 1.000 2 2009 2013
dbSNP: rs34572943
rs34572943
1 1.000 0.080 16 31261032 intron variant G/A snv 0.11 0.700 1.000 2 2015 2017
dbSNP: rs12928725
rs12928725
1 1.000 0.080 16 31272675 intron variant G/A;T snv 0.700 1.000 1 2017 2017
dbSNP: rs35472514
rs35472514
1 1.000 0.080 16 31272002 intron variant C/G;T snv 0.12 0.12 0.700 1.000 1 2015 2015
dbSNP: rs7193268
rs7193268
1 1.000 0.080 16 31329676 intron variant C/T snv 0.20 0.700 1.000 1 2011 2011