Gene: CCND3 ×
Source: ALL
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: rs9349205
rs9349205
CCND3
7 6 41957421 intron variant G/A;C snv 0.800 1.000 3 2009 2018
dbSNP: rs3218097
rs3218097
CCND3
5 6 41937537 intron variant G/A;T snv 0.800 1.000 2 2010 2012
dbSNP: rs112233623
rs112233623
CCND3
5 6 41957260 intron variant C/T snv 7.0E-03 0.700 1.000 2 2016 2019
dbSNP: rs11970772
rs11970772
CCND3
5 6 41957552 intron variant T/A snv 0.24 0.700 1.000 1 2016 2016
dbSNP: rs16895130
rs16895130
CCND3
3 6 41957193 intron variant A/G snv 0.22 0.700 1.000 1 2018 2018
dbSNP: rs182679717
rs182679717
CCND3 ; LOC105375060
1 6 42007955 intron variant C/A;T snv 0.700 1.000 1 2019 2019
dbSNP: rs9296369
rs9296369
CCND3
2 6 41953258 intron variant C/G;T snv 0.700 1.000 1 2016 2016
dbSNP: rs9367125
rs9367125
CCND3 ; LOC105375059
1 6 42019806 intron variant G/C snv 0.10 0.700 1.000 1 2017 2017
dbSNP: rs9369327
rs9369327
CCND3
1 6 42046566 intron variant C/T snv 6.5E-02 0.700 1.000 1 2016 2016
dbSNP: rs9394841
rs9394841
CCND3
3 6 41959197 intron variant T/C snv 0.22 0.700 1.000 1 2016 2016