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: rs11136000
rs11136000
CLU
19 0.752 0.160 8 27607002 intron variant T/C snv 0.56 0.900 0.913 23 2009 2018
dbSNP: rs9331888
rs9331888
5 0.827 0.200 8 27611345 5 prime UTR variant C/G snv 0.35 0.28 0.880 1.000 9 2009 2019
dbSNP: rs2279590
rs2279590
CLU
5 0.851 0.200 8 27598736 non coding transcript exon variant T/C snv 0.69 0.840 1.000 6 2009 2019
dbSNP: rs9331896
rs9331896
4 0.851 0.080 8 27610169 intron variant C/G;T snv 0.820 1.000 6 2013 2019
dbSNP: rs1532278
rs1532278
CLU
2 0.925 0.080 8 27608798 non coding transcript exon variant T/C snv 0.68 0.800 1.000 1 2011 2011
dbSNP: rs4236673
rs4236673
CLU
1 1.000 0.080 8 27607412 intron variant A/G snv 0.70 0.700 1.000 2 2018 2019
dbSNP: rs9331908
rs9331908
CLU
1 1.000 0.080 8 27606101 intron variant C/T snv 0.35 0.700 1.000 1 2018 2018
dbSNP: rs9331942
rs9331942
1 1.000 0.080 8 27597597 3 prime UTR variant A/G snv 7.4E-02 5.6E-02 0.010 1.000 1 2016 2016