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: rs34548439
rs34548439
1 1.000 0.071 5 38831029 intron variant T/A,C snp 0.22 0.700 1 2017 2017
dbSNP: rs35226739
rs35226739
1 1.000 0.071 3 7428456 intron variant T/G snp 1.0E-02 0.700 1 2017 2017
dbSNP: rs6068583
rs6068583
1 1.000 0.071 20 53559566 intron variant A/C snp 0.19 0.700 1 2017 2017
dbSNP: rs7944251
rs7944251
1 1.000 0.071 11 92263265 intergenic variant G/A snp 0.29 0.700 1 2017 2017
dbSNP: rs1805087
rs1805087
MTR
75 0.538 0.679 1 236885200 missense variant A/G snp 0.20 0.21 0.050 1.000 5 1999 2013
dbSNP: rs1801166
rs1801166
APC
12 0.756 0.179 5 112839543 missense variant G/C snp 4.4E-03 4.3E-03 0.040 1.000 4 2001 2009
dbSNP: rs397507444
rs397507444
169 0.457 0.714 1 11794407 missense variant T/G snp 0.030 1.000 3 2004 2007
dbSNP: rs1695
rs1695
100 0.510 0.679 11 67585218 missense variant A/G snp 0.34 0.35 0.020 0.500 2 2006 2012
dbSNP: rs1799853
rs1799853
6 0.846 0.107 10 94942290 missense variant C/T snp 9.2E-02 8.2E-02 0.020 1.000 2 2007 2014
dbSNP: rs1801155
rs1801155
APC
31 0.657 0.393 5 112839514 missense variant T/A snp 2.0E-03; 8.0E-06 6.4E-04 0.020 1.000 2 2005 2006
dbSNP: rs861539
rs861539
60 0.561 0.464 14 103699416 missense variant G/A snp 0.29 0.29 0.020 1.000 2 2005 2006
dbSNP: rs1042028
rs1042028
20 0.685 0.321 16 28606193 missense variant C/T snp 0.22 0.31 0.010 1.000 1 2003 2003
dbSNP: rs1051740
rs1051740
29 0.647 0.429 1 225831932 missense variant T/C snp 0.32 0.28 0.010 < 0.001 1 2012 2012
dbSNP: rs1052133
rs1052133
77 0.533 0.643 3 9757089 missense variant C/G snp 0.27 0.22 0.010 1.000 1 2005 2005
dbSNP: rs1057910
rs1057910
6 0.821 0.143 10 94981296 missense variant A/C,G snp 6.3E-02; 4.0E-06 4.9E-02 0.010 1.000 1 2007 2007
dbSNP: rs10936599
rs10936599
13 0.734 0.393 3 169774313 synonymous variant C/T snp 0.29 0.22 0.010 1.000 1 2012 2012
dbSNP: rs10957057
rs10957057
1 1.000 0.071 8 58487781 intergenic variant C/T snp 0.12 0.010 1.000 1 2012 2012
dbSNP: rs1105879
rs1105879
7 0.821 0.143 2 233693556 missense variant A/C snp 0.35 0.34 0.010 1.000 1 2007 2007
dbSNP: rs1126667
rs1126667
3 0.878 0.107 17 6999441 missense variant A/G snp 0.60 0.61 0.010 1.000 1 2007 2007
dbSNP: rs1130864
rs1130864
CRP
17 0.707 0.321 1 159713301 3 prime UTR variant G/A snp 0.26 0.010 1.000 1 2010 2010
dbSNP: rs113193886
rs113193886
38 0.608 0.464 7 143267671 missense variant A/T snp 4.0E-06 0.010 < 0.001 1 2012 2012
dbSNP: rs1138272
rs1138272
16 0.699 0.286 11 67586108 missense variant C/T snp 5.9E-02 6.1E-02 0.010 < 0.001 1 2012 2012
dbSNP: rs11540654
rs11540654
117 0.492 0.679 17 7676040 missense variant C/A,G,T snp 4.8E-05 3.2E-05 0.010 1.000 1 2006 2006
dbSNP: rs11786580
rs11786580
1 1.000 0.071 8 58493381 intron variant C/T snp 0.18 0.010 1.000 1 2012 2012
dbSNP: rs1205
rs1205
CRP
30 0.652 0.500 1 159712443 3 prime UTR variant C/T snp 0.32 0.010 1.000 1 2010 2010