Source: GWASCAT

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs56144648
rs56144648
CCND3 ; LOC105375059
6 42021004 intron variant G/A snv 0.18
CUI: C0001948
Disease: Alcohol consumption
Alcohol consumption 		0.700 1.000 1 2019 2019
dbSNP: rs3218097
rs3218097
CCND3
6 41937537 intron variant G/A;T snv
CUI: C4528257
Disease: Corpuscular Hemoglobin Concentration Mean
Corpuscular Hemoglobin Concentration Mean 		0.800 1.000 1 2012 2017
dbSNP: rs67289879
rs67289879
CCND3
1.000 0.040 6 42039665 intron variant C/A;G;T snv
CUI: C0010346
Disease: Crohn Disease
Crohn Disease 		0.700 1.000 1 2017 2017
dbSNP: rs9381118
rs9381118
CCND3 ; LOC105375059
6 42017698 intron variant T/C snv 0.72
CUI: C0200638
Disease: Eosinophil count procedure
Eosinophil count procedure 		0.700 1.000 1 2019 2019
dbSNP: rs9349205
rs9349205
CCND3
6 41957421 intron variant G/A;C snv
CUI: C1261502
Disease: Finding of Mean Corpuscular Hemoglobin
Finding of Mean Corpuscular Hemoglobin 		0.800 1.000 3 2009 2018
dbSNP: rs112233623
rs112233623
CCND3
6 41957260 intron variant C/T snv 7.0E-03
CUI: C1261502
Disease: Finding of Mean Corpuscular Hemoglobin
Finding of Mean Corpuscular Hemoglobin 		0.700 1.000 2 2016 2019
dbSNP: rs11970772
rs11970772
CCND3
6 41957552 intron variant T/A snv 0.24
CUI: C1261502
Disease: Finding of Mean Corpuscular Hemoglobin
Finding of Mean Corpuscular Hemoglobin 		0.700 1.000 1 2016 2016
dbSNP: rs16895130
rs16895130
CCND3
6 41957193 intron variant A/G snv 0.22
CUI: C1261502
Disease: Finding of Mean Corpuscular Hemoglobin
Finding of Mean Corpuscular Hemoglobin 		0.700 1.000 1 2018 2018
dbSNP: rs182679717
rs182679717
CCND3 ; LOC105375060
6 42007955 intron variant C/A;T snv
CUI: C1261502
Disease: Finding of Mean Corpuscular Hemoglobin
Finding of Mean Corpuscular Hemoglobin 		0.700 1.000 1 2019 2019
dbSNP: rs3218097
rs3218097
CCND3
6 41937537 intron variant G/A;T snv
CUI: C1261502
Disease: Finding of Mean Corpuscular Hemoglobin
Finding of Mean Corpuscular Hemoglobin 		0.800 1.000 1 2010 2012
dbSNP: rs9296369
rs9296369
CCND3
6 41953258 intron variant C/G;T snv
CUI: C1261502
Disease: Finding of Mean Corpuscular Hemoglobin
Finding of Mean Corpuscular Hemoglobin 		0.700 1.000 1 2016 2016
dbSNP: rs9367125
rs9367125
CCND3 ; LOC105375059
6 42019806 intron variant G/C snv 0.10
CUI: C1261502
Disease: Finding of Mean Corpuscular Hemoglobin
Finding of Mean Corpuscular Hemoglobin 		0.700 1.000 1 2017 2017
dbSNP: rs9369327
rs9369327
CCND3
6 42046566 intron variant C/T snv 6.5E-02
CUI: C1261502
Disease: Finding of Mean Corpuscular Hemoglobin
Finding of Mean Corpuscular Hemoglobin 		0.700 1.000 1 2016 2016
dbSNP: rs9394841
rs9394841
CCND3
6 41959197 intron variant T/C snv 0.22
CUI: C1261502
Disease: Finding of Mean Corpuscular Hemoglobin
Finding of Mean Corpuscular Hemoglobin 		0.700 1.000 1 2016 2016
dbSNP: rs3218097
rs3218097
CCND3
6 41937537 intron variant G/A;T snv
CUI: C0518015
Disease: Hemoglobin measurement
Hemoglobin measurement 		0.700 1.000 1 2010 2010
dbSNP: rs4130023
rs4130023
CCND3
6 41966776 intron variant C/T snv 0.17
CUI: C0392885
Disease: High density lipoprotein measurement
High density lipoprotein measurement 		0.700 1.000 1 2018 2018
dbSNP: rs4714556
rs4714556
CCND3
6 42025491 intron variant A/G snv 0.39
CUI: C0392885
Disease: High density lipoprotein measurement
High density lipoprotein measurement 		0.700 1.000 1 2017 2017
dbSNP: rs56144648
rs56144648
CCND3 ; LOC105375059
6 42021004 intron variant G/A snv 0.18
CUI: C0392885
Disease: High density lipoprotein measurement
High density lipoprotein measurement 		0.700 1.000 1 2019 2019
dbSNP: rs67289879
rs67289879
CCND3
1.000 0.040 6 42039665 intron variant C/A;G;T snv
CUI: C0021390
Disease: Inflammatory Bowel Diseases
Inflammatory Bowel Diseases 		0.700 1.000 1 2017 2017
dbSNP: rs33966734
rs33966734
CCND3
6 41936060 stop gained C/A;G;T snv 1.2E-02; 4.0E-06
CUI: C0424678
Disease: Lean body mass
Lean body mass 		0.700 1.000 1 2019 2019
dbSNP: rs9349205
rs9349205
CCND3
6 41957421 intron variant G/A;C snv
CUI: C0524587
Disease: Mean Corpuscular Volume (result)
Mean Corpuscular Volume (result) 		0.800 1.000 4 2009 2018
dbSNP: rs112233623
rs112233623
CCND3
6 41957260 intron variant C/T snv 7.0E-03
CUI: C0524587
Disease: Mean Corpuscular Volume (result)
Mean Corpuscular Volume (result) 		0.700 1.000 2 2016 2016
dbSNP: rs11970772
rs11970772
CCND3
6 41957552 intron variant T/A snv 0.24
CUI: C0524587
Disease: Mean Corpuscular Volume (result)
Mean Corpuscular Volume (result) 		0.700 1.000 2 2009 2016
dbSNP: rs3218097
rs3218097
CCND3
6 41937537 intron variant G/A;T snv
CUI: C0524587
Disease: Mean Corpuscular Volume (result)
Mean Corpuscular Volume (result) 		0.800 1.000 2 2010 2013
dbSNP: rs16895130
rs16895130
CCND3
6 41957193 intron variant A/G snv 0.22
CUI: C0524587
Disease: Mean Corpuscular Volume (result)
Mean Corpuscular Volume (result) 		0.700 1.000 1 2018 2018