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: 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: 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: 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: 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
dbSNP: rs4714548
rs4714548
CCND3 ; LOC105375059
6 42015693 intron variant A/C;G;T snv
CUI: C0524587
Disease: Mean Corpuscular Volume (result)
Mean Corpuscular Volume (result) 		0.700 1.000 1 2017 2017
dbSNP: rs9296369
rs9296369
CCND3
6 41953258 intron variant C/G;T snv
CUI: C0524587
Disease: Mean Corpuscular Volume (result)
Mean Corpuscular Volume (result) 		0.700 1.000 1 2016 2016
dbSNP: rs9349204
rs9349204
CCND3
6 41946640 intron variant A/G;T snv
CUI: C0524587
Disease: Mean Corpuscular Volume (result)
Mean Corpuscular Volume (result) 		0.700 1.000 1 2012 2012