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: rs6265
rs6265
171 0.463 0.679 11 27658369 missense variant C/T snp 0.19 0.15 0.100 0.982 56 2005 2018
dbSNP: rs759834365
rs759834365
157 0.471 0.679 11 27658456 missense variant C/T snp 1.2E-05 0.100 0.981 53 2005 2018
dbSNP: rs4680
rs4680
155 0.484 0.821 22 19963748 missense variant G/A snp 0.46 0.45 0.100 0.833 12 2008 2015
dbSNP: rs25531
rs25531
39 0.626 0.321 17 30237328 intergenic variant T/C snp 0.070 0.857 7 2009 2016
dbSNP: rs2522833
rs2522833
6 0.821 0.071 7 82824392 missense variant A/C snp 0.45 0.35 0.040 0.750 4 2010 2015
dbSNP: rs5443
rs5443
65 0.570 0.571 12 6845711 synonymous variant C/T snp 0.36 0.43 0.040 1.000 4 2004 2018
dbSNP: rs6313
rs6313
50 0.590 0.500 13 46895805 synonymous variant G/A snp 0.41 0.39 0.040 1.000 4 2007 2015
dbSNP: rs53576
rs53576
23 0.692 0.107 3 8762685 intron variant A/G,T snp 0.67 0.030 1.000 3 2014 2018
dbSNP: rs5522
rs5522
15 0.734 0.286 4 148436323 missense variant C/T snp 0.88 0.89 0.030 1.000 3 2010 2016
dbSNP: rs7103411
rs7103411
12 0.784 0.107 11 27678578 intron variant C/T snp 0.82 0.030 1.000 3 2010 2016
dbSNP: rs9340799
rs9340799
37 0.611 0.607 6 151842246 intron variant A/G snp 0.31 0.030 1.000 3 2011 2018
dbSNP: rs1130864
rs1130864
CRP
17 0.707 0.321 1 159713301 3 prime UTR variant G/A snp 0.26 0.020 0.500 2 2009 2015
dbSNP: rs1187323
rs1187323
3 0.923 0.071 9 84668501 regulatory region variant C/A,G,T snp 0.81; 3.2E-05 0.020 1.000 2 2010 2016
dbSNP: rs1205
rs1205
CRP
30 0.652 0.500 1 159712443 3 prime UTR variant C/T snp 0.32 0.020 1.000 2 2009 2015
dbSNP: rs1360780
rs1360780
16 0.769 0.107 6 35639794 intron variant T/A,C snp 0.69 0.020 0.500 2 2012 2015
dbSNP: rs16139
rs16139
27 0.657 0.500 7 24285260 missense variant T/A,C snp 4.0E-06; 3.0E-02 3.2E-02 0.020 1.000 2 2009 2013
dbSNP: rs2230912
rs2230912
10 0.769 0.143 12 121184393 missense variant A/G snp 0.13 0.12 0.020 1.000 2 2009 2010
dbSNP: rs6295
rs6295
32 0.667 0.179 5 63962738 intron variant C/G snp 0.49 0.020 1.000 2 2011 2015
dbSNP: rs662
rs662
71 0.561 0.607 7 95308134 missense variant T/C snp 0.38 0.41 0.020 0.500 2 2007 2010
dbSNP: rs9939609
rs9939609
FTO
74 0.580 0.607 16 53786615 intron variant T/A snp 0.42 0.020 0.500 2 2014 2016
dbSNP: rs1006737
rs1006737
31 0.679 0.107 12 2236129 intron variant G/A snp 0.37 0.010 1.000 1 2010 2010
dbSNP: rs1013940
rs1013940
3 0.878 0.071 2 107992192 missense variant A/G snp 9.3E-02 7.4E-02 0.010 1.000 1 2008 2008
dbSNP: rs10410544
rs10410544
3 0.878 0.107 19 38894892 intron variant T/C snp 0.68 0.66 0.010 1.000 1 2014 2014
dbSNP: rs10434
rs10434
8 0.769 0.286 6 43785475 3 prime UTR variant A/G snp 0.59 0.010 1.000 1 2015 2015
dbSNP: rs1049353
rs1049353
26 0.657 0.464 6 88143916 synonymous variant C/T snp 0.21 0.20 0.010 1.000 1 2012 2012