Gene: CR1 ×
Source: ALL
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
8 0.776 0.200 1 207518704 intron variant A/G;T snv 0.900 1.000 17 2009 2019
dbSNP: rs3818361
rs3818361
CR1
6 0.851 0.080 1 207611623 intron variant A/G snv 0.74 0.880 1.000 11 2009 2017
dbSNP: rs6701713
rs6701713
CR1
1 1.000 0.080 1 207612944 intron variant A/G;T snv 0.810 1.000 3 2011 2018
dbSNP: rs4844610
rs4844610
CR1
1 1.000 0.080 1 207629207 intron variant A/C snv 0.87 0.710 1.000 2 2011 2012
dbSNP: rs12036785
rs12036785
CR1
1 1.000 0.080 1 207619564 intron variant C/A snv 0.47 0.700 1.000 1 2018 2018
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: rs2093760
rs2093760
CR1
1 1.000 0.080 1 207613483 intron variant A/G snv 0.74 0.700 1.000 1 2019 2019
dbSNP: rs2296160
rs2296160
CR1
2 0.925 0.120 1 207621975 missense variant A/G snv 0.82 0.81 0.700 1.000 1 2011 2011
dbSNP: rs679515
rs679515
CR1
1 1.000 0.080 1 207577223 intron variant T/A;C snv 0.700 1.000 1 2016 2016
dbSNP: rs1344800847
rs1344800847
CR1
2 0.925 0.120 1 207569911 missense variant G/T snv 0.010 1.000 1 2018 2018
dbSNP: rs3738467
rs3738467
CR1
2 0.925 0.120 1 207552816 missense variant G/T snv 1.4E-03 0.010 1.000 1 2018 2018
dbSNP: rs4844609
rs4844609
CR1
1 1.000 0.080 1 207609571 missense variant A/T snv 0.99 0.99 0.010 1.000 1 2013 2013