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: rs6656401
rs6656401
CR1
1 0.776 0.200 1 207518704 intron variant A/G;T snv 0.900 1.000 3 2009 2019
dbSNP: rs3818361
rs3818361
CR1
1 0.851 0.080 1 207611623 intron variant A/G snv 0.74 0.880 1.000 3 2009 2017
dbSNP: rs6701713
rs6701713
CR1
1 1.000 0.080 1 207612944 intron variant A/G;T snv 0.810 1.000 1 2011 2018
dbSNP: rs4844610
rs4844610
CR1
1 1.000 0.080 1 207629207 intron variant A/C snv 0.87 0.710 1.000 1 2011 2012
dbSNP: rs1408077
rs1408077
CR1
1 1.000 0.080 1 207630796 intron variant A/C snv 0.84 0.700 1.000 1 2011 2011
dbSNP: rs1408078
rs1408078
CR1
1 1.000 0.080 1 207627210 intron variant T/C snv 0.84 0.700 1.000 1 2011 2011
dbSNP: rs2296160
rs2296160
CR1
1 0.925 0.120 1 207621975 missense variant A/G snv 0.82 0.81 0.700 1.000 1 2011 2011