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: rs121918616
rs121918616
3 0.882 0.080 1 160130283 missense variant G/A snv 4.0E-06 0.010 1.000 1 2005 2005
dbSNP: rs1402027664
rs1402027664
2 0.925 0.080 19 13312697 missense variant T/C snv 0.010 1.000 1 2005 2005
dbSNP: rs886039322
rs886039322
2 1.000 0.080 19 13312778 missense variant T/C snv 8.9E-06 7.0E-06 0.010 < 0.001 1 2005 2005
dbSNP: rs1553245943
rs1553245943
2 1.000 0.080 1 160137001 missense variant G/A snv 0.700 1.000 4 2008 2017
dbSNP: rs121918628
rs121918628
5 0.851 0.080 2 165998049 missense variant G/T snv 0.020 1.000 2 2008 2013
dbSNP: rs41276886
rs41276886
2 0.925 0.080 19 13317310 missense variant C/T snv 4.5E-03 4.4E-03 0.010 1.000 1 2010 2010
dbSNP: rs759252101
rs759252101
1 1.000 0.080 19 13212143 missense variant C/G snv 4.0E-06 0.010 < 0.001 1 2012 2012
dbSNP: rs121918799
rs121918799
14 0.752 0.120 2 166015636 missense variant G/C snv 1.7E-03 1.6E-03 0.010 1.000 1 2013 2013
dbSNP: rs746795369
rs746795369
6 0.827 0.080 1 160139969 missense variant C/A;T snv 1.2E-05; 4.0E-06 0.010 1.000 1 2013 2013
dbSNP: rs1026872132
rs1026872132
1 1.000 0.080 19 13234934 missense variant T/C snv 7.0E-06 0.010 1.000 1 2016 2016
dbSNP: rs376885324
rs376885324
1 1.000 0.080 2 165996096 missense variant T/C snv 0.010 1.000 1 2016 2016
dbSNP: rs121918632
rs121918632
5 0.851 0.120 2 165996099 missense variant A/G snv 7.0E-06 0.010 1.000 1 2018 2018