Variant DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Disease Class Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs1805096
rs1805096
0.878 0.143 1 65636574 synonymous variant G/A snp 0.46 0.44
CUI: C0201657
Disease: C-reactive protein measurement
C-reactive protein measurement
0.800 3 2012 2013
dbSNP: rs6700896
rs6700896
0.821 0.143 1 65624099 intron variant C/T snp 0.44
CUI: C0201657
Disease: C-reactive protein measurement
C-reactive protein measurement
0.800 2 2009 2013
dbSNP: rs10889569
rs10889569
1 65620511 intron variant A/T snp 0.47
CUI: C0201657
Disease: C-reactive protein measurement
C-reactive protein measurement
0.800 1 2013 2013
dbSNP: rs11208659
rs11208659
1.000 0.071 1 65513597 intron variant T/C snp 0.16
CUI: C0028754
Disease: Obesity
Obesity
Nutritional and Metabolic Diseases; Pathological Conditions, Signs and Symptoms 0.800 1 2013 2013
dbSNP: rs17127608
rs17127608
1 65428258 intron variant C/T snp 3.8E-02
Low density lipoprotein cholesterol measurement
0.700 1 2012 2012
dbSNP: rs201721079
rs201721079
1 65615104 intron variant T/TC in-del
CUI: C0201657
Disease: C-reactive protein measurement
C-reactive protein measurement
0.700 1 2013 2013
dbSNP: rs34499590
rs34499590
1 65616108 missense variant C/G,T snp 2.5E-03 1.0E-02
Low density lipoprotein cholesterol measurement
0.700 1 2012 2012
dbSNP: rs34499590
rs34499590
1 65616108 missense variant C/G,T snp 2.5E-03 1.0E-02
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement
0.700 1 2012 2012
dbSNP: rs35308591
rs35308591
1 65615105 intron variant C/CC in-del
CUI: C0201657
Disease: C-reactive protein measurement
C-reactive protein measurement
0.700 1 2013 2013
dbSNP: rs4655537
rs4655537
1 65593118 intron variant A/G,T snp 0.66
CUI: C0201657
Disease: C-reactive protein measurement
C-reactive protein measurement
0.700 1 2013 2013
dbSNP: rs4655555
rs4655555
1 65614586 intron variant T/A snp 0.24
CUI: C0201657
Disease: C-reactive protein measurement
C-reactive protein measurement
0.700 1 2013 2013
dbSNP: rs4655557
rs4655557
1 65615104 intron variant T/A,C snp 0.47
CUI: C0201657
Disease: C-reactive protein measurement
C-reactive protein measurement
0.700 1 2013 2013
dbSNP: rs6588153
rs6588153
1 65626334 intron variant T/A snp 0.44
CUI: C0201657
Disease: C-reactive protein measurement
C-reactive protein measurement
0.700 1 2013 2013
dbSNP: rs6678033
rs6678033
1 65611941 intron variant G/A snp 0.46
CUI: C0201657
Disease: C-reactive protein measurement
C-reactive protein measurement
0.700 1 2013 2013
dbSNP: rs6690625
rs6690625
1 65611907 intron variant T/G snp 0.31
CUI: C0201657
Disease: C-reactive protein measurement
C-reactive protein measurement
0.700 1 2013 2013
dbSNP: rs6700896
rs6700896
0.821 0.143 1 65624099 intron variant C/T snp 0.44
CUI: C0524587
Disease: Mean Corpuscular Volume (result)
Mean Corpuscular Volume (result)
0.700 1 2017 2017
dbSNP: rs6700896
rs6700896
0.821 0.143 1 65624099 intron variant C/T snp 0.44
Erythrocyte Mean Corpuscular Hemoglobin Test
0.700 1 2017 2017
dbSNP: rs6700896
rs6700896
0.821 0.143 1 65624099 intron variant C/T snp 0.44
Finding of Mean Corpuscular Hemoglobin
0.700 1 2017 2017
dbSNP: rs7516341
rs7516341
1 65622460 intron variant T/C snp 0.47
CUI: C0201657
Disease: C-reactive protein measurement
C-reactive protein measurement
0.700 1 2013 2013
dbSNP: rs9436735
rs9436735
1 65419378 intergenic variant C/G snp 2.4E-02
High density lipoprotein measurement
0.700 1 2012 2012
dbSNP: rs9436735
rs9436735
1 65419378 intergenic variant C/G snp 2.4E-02
Low density lipoprotein cholesterol measurement
0.700 1 2012 2012
dbSNP: rs9436735
rs9436735
1 65419378 intergenic variant C/G snp 2.4E-02
CUI: C1445957
Disease: Serum total cholesterol measurement
Serum total cholesterol measurement
0.700 1 2012 2012
dbSNP: rs9436742
rs9436742
1 65432648 3 prime UTR variant C/T snp 2.3E-02
Low density lipoprotein cholesterol measurement
0.700 1 2012 2012
dbSNP: rs9436747
rs9436747
1 65445924 intron variant T/C snp 0.54
CUI: C0200641
Disease: Blood basophil count (lab test)
Blood basophil count (lab test)
0.700 1 2017 2017
dbSNP: rs9436747
rs9436747
1 65445924 intron variant T/C snp 0.54
CUI: C0200633
Disease: Neutrophil count (procedure)
Neutrophil count (procedure)
0.700 1 2017 2017