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: rs2794520
rs2794520
9 0.807 0.240 1 159709026 upstream gene variant C/A;T snv 0.800 1.000 8 2007 2019
dbSNP: rs7553007
rs7553007
7 0.827 0.120 1 159728759 intergenic variant G/A snv 0.31 0.800 1.000 8 2009 2019
dbSNP: rs1341665
rs1341665
2 1.000 0.080 1 159721769 intergenic variant G/A snv 0.32 0.800 1.000 6 2012 2019
dbSNP: rs1205
rs1205
CRP
46 0.602 0.680 1 159712443 3 prime UTR variant C/T snv 0.30 0.700 1.000 5 2012 2014
dbSNP: rs12068753
rs12068753
2 1.000 0.120 1 159722747 intergenic variant T/A snv 0.15 0.800 1.000 5 2012 2015
dbSNP: rs1805096
rs1805096
6 0.827 0.200 1 65636574 synonymous variant G/A snv 0.46 0.43 0.800 1.000 5 2012 2019
dbSNP: rs16842559
rs16842559
1 1 159706381 upstream gene variant T/C snv 5.6E-02 0.800 1.000 4 2012 2019
dbSNP: rs2027471
rs2027471
1 1 159719598 intergenic variant T/A snv 0.32 0.700 1.000 4 2012 2014
dbSNP: rs2808628
rs2808628
2 1 159706221 upstream gene variant G/A snv 0.31 0.700 1.000 4 2012 2014
dbSNP: rs2808629
rs2808629
3 0.925 0.160 1 159707006 upstream gene variant G/A snv 0.31 0.700 1.000 4 2012 2014
dbSNP: rs3091244
rs3091244
CRP
17 0.724 0.280 1 159714875 upstream gene variant G/A;T snv 0.800 1.000 4 2008 2018
dbSNP: rs4129267
rs4129267
13 0.807 0.200 1 154453788 intron variant C/G;T snv 0.800 1.000 4 2011 2019
dbSNP: rs876537
rs876537
3 1.000 0.080 1 159705143 non coding transcript exon variant C/T snv 0.34 0.800 1.000 4 2012 2019
dbSNP: rs10494326
rs10494326
1 1 159679910 intergenic variant C/T snv 5.3E-02 0.800 1.000 3 2012 2019
dbSNP: rs11265257
rs11265257
1 1 159699194 intergenic variant C/T snv 0.34 0.700 1.000 3 2012 2013
dbSNP: rs11265260
rs11265260
2 1.000 0.080 1 159730249 intergenic variant A/G snv 6.8E-02 0.800 1.000 3 2012 2019
dbSNP: rs12081252
rs12081252
1 1 159736723 intergenic variant T/C snv 7.6E-02 0.700 1.000 3 2012 2014
dbSNP: rs12081264
rs12081264
1 1 159736770 intergenic variant T/C snv 0.15 0.700 1.000 3 2012 2014
dbSNP: rs12239046
rs12239046
9 1 247438293 intron variant T/C snv 0.58 0.800 1.000 3 2011 2019
dbSNP: rs1470515
rs1470515
1 1 159683809 intergenic variant C/T snv 0.36 0.700 1.000 3 2012 2013
dbSNP: rs16842502
rs16842502
1 1 159684073 intergenic variant C/A snv 5.5E-02 0.700 1.000 3 2012 2014
dbSNP: rs16842568
rs16842568
1 1 159706430 upstream gene variant A/G snv 5.6E-02 0.700 1.000 3 2012 2014
dbSNP: rs16842599
rs16842599
1 1 159727685 intergenic variant T/C snv 7.4E-02 0.700 1.000 3 2012 2014
dbSNP: rs1892534
rs1892534
7 0.925 0.120 1 65640261 3 prime UTR variant C/T snv 0.44 0.800 1.000 3 2008 2019
dbSNP: rs2228145
rs2228145
57 0.602 0.720 1 154454494 missense variant A/C;T snv 0.38; 1.2E-05 0.800 1.000 3 2008 2019