Source: GWASDB

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: 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: rs10947997
rs10947997
CCND3
6 41953503 intron variant G/T snv 0.13
CUI: C0014772
Disease: Red Blood Cell Count measurement
Red Blood Cell Count measurement 		0.800 1.000 1 2009 2016
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: rs3218097
rs3218097
CCND3
6 41937537 intron variant G/A;T snv
CUI: C0014772
Disease: Red Blood Cell Count measurement
Red Blood Cell Count measurement 		0.800 1.000 1 2009 2010
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: 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 1 2009 2018
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 1 2009 2018
dbSNP: rs1051130
rs1051130
CCND3
6 41936044 missense variant A/C;G;T snv 0.54; 1.6E-05
CUI: C0014772
Disease: Red Blood Cell Count measurement
Red Blood Cell Count measurement 		0.700 1.000 1 2009 2009
dbSNP: rs10947997
rs10947997
CCND3
6 41953503 intron variant G/T snv 0.13
CUI: C0524587
Disease: Mean Corpuscular Volume (result)
Mean Corpuscular Volume (result) 		0.700 1.000 1 2012 2012
dbSNP: rs10947997
rs10947997
CCND3
6 41953503 intron variant G/T snv 0.13
CUI: C4528257
Disease: Corpuscular Hemoglobin Concentration Mean
Corpuscular Hemoglobin Concentration Mean 		0.700 1.000 1 2012 2012
dbSNP: rs11756584
rs11756584
CCND3 ; LOC105375059
6 42010199 intron variant G/A snv 0.33
CUI: C4528257
Disease: Corpuscular Hemoglobin Concentration Mean
Corpuscular Hemoglobin Concentration Mean 		0.700 1.000 1 2012 2012
dbSNP: rs11968166
rs11968166
CCND3
6 41957566 intron variant G/A snv 0.18
CUI: C0014772
Disease: Red Blood Cell Count measurement
Red Blood Cell Count measurement 		0.700 1.000 1 2009 2009
dbSNP: rs11968166
rs11968166
CCND3
6 41957566 intron variant G/A snv 0.18
CUI: C4528257
Disease: Corpuscular Hemoglobin Concentration Mean
Corpuscular Hemoglobin Concentration Mean 		0.700 1.000 1 2012 2012
dbSNP: rs11970772
rs11970772
CCND3
6 41957552 intron variant T/A snv 0.24
CUI: C0023508
Disease: White Blood Cell Count procedure
White Blood Cell Count procedure 		0.700 1.000 1 2009 2009
dbSNP: rs11970772
rs11970772
CCND3
6 41957552 intron variant T/A snv 0.24
CUI: C0014772
Disease: Red Blood Cell Count measurement
Red Blood Cell Count measurement 		0.700 1.000 1 2009 2009
dbSNP: rs11970772
rs11970772
CCND3
6 41957552 intron variant T/A snv 0.24
CUI: C4528257
Disease: Corpuscular Hemoglobin Concentration Mean
Corpuscular Hemoglobin Concentration Mean 		0.700 1.000 1 2012 2012
dbSNP: rs12214723
rs12214723
CCND3
6 42025950 intron variant G/A snv 0.20
CUI: C4528257
Disease: Corpuscular Hemoglobin Concentration Mean
Corpuscular Hemoglobin Concentration Mean 		0.700 1.000 1 2012 2012
dbSNP: rs16895128
rs16895128
CCND3
6 41956631 intron variant G/A snv 0.19
CUI: C0014772
Disease: Red Blood Cell Count measurement
Red Blood Cell Count measurement 		0.700 1.000 1 2009 2009
dbSNP: rs16895128
rs16895128
CCND3
6 41956631 intron variant G/A snv 0.19
CUI: C4528257
Disease: Corpuscular Hemoglobin Concentration Mean
Corpuscular Hemoglobin Concentration Mean 		0.700 1.000 1 2012 2012
dbSNP: rs16895130
rs16895130
CCND3
6 41957193 intron variant A/G snv 0.22
CUI: C4528257
Disease: Corpuscular Hemoglobin Concentration Mean
Corpuscular Hemoglobin Concentration Mean 		0.700 1.000 1 2012 2012
dbSNP: rs2479720
rs2479720
CCND3
6 41947966 intron variant G/C snv 0.81
CUI: C4528257
Disease: Corpuscular Hemoglobin Concentration Mean
Corpuscular Hemoglobin Concentration Mean 		0.700 1.000 1 2012 2012
dbSNP: rs3218086
rs3218086
CCND3
6 41942326 intron variant C/T snv 0.18
CUI: C0014772
Disease: Red Blood Cell Count measurement
Red Blood Cell Count measurement 		0.700 1.000 1 2009 2009
dbSNP: rs3218086
rs3218086
CCND3
6 41942326 intron variant C/T snv 0.18
CUI: C4528257
Disease: Corpuscular Hemoglobin Concentration Mean
Corpuscular Hemoglobin Concentration Mean 		0.700 1.000 1 2012 2012
dbSNP: rs3218108
rs3218108
CCND3
6 41934917 downstream gene variant C/T snv 0.19
CUI: C4528257
Disease: Corpuscular Hemoglobin Concentration Mean
Corpuscular Hemoglobin Concentration Mean 		0.700 1.000 1 2012 2012
dbSNP: rs3218108
rs3218108
CCND3
6 41934917 downstream gene variant C/T snv 0.19
CUI: C0014772
Disease: Red Blood Cell Count measurement
Red Blood Cell Count measurement 		0.700 1.000 1 2009 2009