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: rs1925690
rs1925690
7 0.784 0.071 6 87157345 intron variant T/A,C snp 0.92 0.700 1 2012 2012
dbSNP: rs749005
rs749005
7 0.784 0.071 6 6283433 intron variant G/T snp 0.14 0.700 1 2012 2012
dbSNP: rs11136000
rs11136000
CLU
10 0.744 0.179 8 27607002 intron variant T/C snp 0.57 0.090 1.000 9 2010 2015
dbSNP: rs3851179
rs3851179
8 0.769 0.214 11 86157598 intergenic variant T/C snp 0.69 0.080 1.000 8 2010 2015
dbSNP: rs10524523
rs10524523
7 0.784 0.179 19 44899792 intron variant CTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT/C. microsatellite 0.070 1.000 7 2011 2016
dbSNP: rs4877365
rs4877365
4 0.846 0.107 9 87540777 intron variant G/A snp 0.28 0.030 1.000 3 2006 2013
dbSNP: rs4878104
rs4878104
4 0.846 0.107 9 87578076 intron variant C/T snp 0.39 0.030 1.000 3 2006 2013
dbSNP: rs5984894
rs5984894
2 0.923 0.071 X 92138738 intron variant A/G snp 0.53 0.030 1.000 3 2009 2011
dbSNP: rs6656401
rs6656401
CR1
7 0.784 0.179 1 207518704 intron variant A/G,T snp 0.86 0.030 1.000 3 2011 2016
dbSNP: rs75932628
rs75932628
22 0.679 0.250 6 41161514 missense variant C/A,T snp 6.8E-05; 2.6E-03 1.5E-03 0.030 1.000 3 2013 2016
dbSNP: rs764929617
rs764929617
7 0.801 0.179 19 44907799 missense variant C/T snp 4.0E-06 0.030 0.667 3 2003 2014
dbSNP: rs10997477
rs10997477
1 1.000 0.071 10 67000961 intron variant C/T snp 0.30 0.020 1.000 2 2012 2014
dbSNP: rs11754661
rs11754661
5 0.846 0.107 6 150885942 intron variant G/A,T snp 4.9E-02 0.020 1.000 2 2011 2012
dbSNP: rs137875858
rs137875858
3 0.878 0.107 4 95170280 missense variant G/A snp 2.9E-04 1.6E-04 0.020 1.000 2 2015 2016
dbSNP: rs1532278
rs1532278
CLU
2 0.923 0.071 8 27608798 non coding transcript exon variant T/C snp 0.68 0.020 1.000 2 2011 2014
dbSNP: rs16923760
rs16923760
1 1.000 0.071 10 66920370 intron variant T/C snp 0.12 0.020 1.000 2 2012 2014
dbSNP: rs17070145
rs17070145
6 0.821 0.071 5 168418786 intron variant C/T snp 0.44 0.020 0.500 2 2011 2018
dbSNP: rs1799983
rs1799983
138 0.475 0.786 7 150999023 missense variant T/A,G snp 0.75 0.76 0.020 1.000 2 2001 2010
dbSNP: rs1925608
rs1925608
1 1.000 0.071 10 66990654 intron variant A/C snp 0.49 0.020 0.500 2 2012 2014
dbSNP: rs1925609
rs1925609
1 1.000 0.071 10 66995149 intron variant T/C snp 0.52 0.020 1.000 2 2012 2014
dbSNP: rs1937
rs1937
1 1.000 0.071 10 58385582 missense variant G/C snp 9.6E-02 8.0E-02 0.020 1.000 2 2008 2012
dbSNP: rs2986017
rs2986017
3 0.878 0.107 10 103458495 missense variant A/G snp 0.79 0.80 0.020 1.000 2 2009 2010
dbSNP: rs3818361
rs3818361
CR1
4 0.846 0.107 1 207611623 intron variant A/G snp 0.73 0.020 1.000 2 2010 2012
dbSNP: rs576980684
rs576980684
3 0.878 0.107 10 103458498 missense variant G/A snp 8.1E-06 0.020 1.000 2 2010 2010
dbSNP: rs5882
rs5882
9 0.784 0.143 16 56982180 missense variant G/A,C snp 0.62 0.59 0.020 1.000 2 2012 2015