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: rs1061170
rs1061170
CFH
72 0.561 0.720 1 196690107 missense variant C/T snv 0.68 0.64 0.010 1.000 1 2015 2015
dbSNP: rs11214105
rs11214105
2 1.000 0.120 11 112166930 intron variant G/A snv 0.25 0.010 1.000 1 2015 2015
dbSNP: rs1205738080
rs1205738080
1 1.000 0.120 10 90857570 synonymous variant G/A snv 4.9E-06 0.010 1.000 1 2008 2008
dbSNP: rs1923884
rs1923884
2 1.000 0.120 13 46847701 intron variant C/T snv 0.12 0.010 1.000 1 2008 2008
dbSNP: rs2247215
rs2247215
1 1.000 0.120 6 101518578 intron variant A/G snv 0.26 0.010 1.000 1 2011 2011
dbSNP: rs25531
rs25531
72 0.581 0.520 17 30237328 upstream gene variant T/C snv 0.18 0.010 1.000 1 2015 2015
dbSNP: rs356653
rs356653
1 1.000 0.120 2 100923328 intron variant G/A;C snv 0.36 0.010 1.000 1 2011 2011
dbSNP: rs369729113
rs369729113
1 1.000 0.120 7 155071001 synonymous variant C/G;T snv 2.0E-05 0.010 1.000 1 2008 2008
dbSNP: rs4151667
rs4151667
9 0.790 0.320 6 31946247 missense variant T/A snv 3.9E-02 3.4E-02 0.010 1.000 1 2015 2015
dbSNP: rs4680
rs4680
249 0.442 0.920 22 19963748 missense variant G/A snv 0.46 0.44 0.010 1.000 1 2015 2015
dbSNP: rs6311
rs6311
41 0.645 0.640 13 46897343 upstream gene variant C/T snv 0.40 0.010 1.000 1 2011 2011
dbSNP: rs6313
rs6313
82 0.562 0.640 13 46895805 synonymous variant G/A snv 0.41 0.40 0.010 1.000 1 2008 2008
dbSNP: rs763780
rs763780
87 0.531 0.720 6 52236941 missense variant T/C snv 6.7E-02 6.6E-02 0.010 1.000 1 2008 2008
dbSNP: rs821616
rs821616
13 0.752 0.200 1 232008852 missense variant A/T snv 0.26 0.29 0.010 1.000 1 2010 2010