Gene: CCND2 ×
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: rs3217810
rs3217810
CCND2
10 0.776 0.080 12 4279105 intron variant C/T snv 8.7E-02 0.700 1.000 4 2013 2019
dbSNP: rs3217874
rs3217874
CCND2
10 0.776 0.080 12 4291642 intron variant C/T snv 0.37 0.700 1.000 1 2019 2019
dbSNP: rs3217901
rs3217901
CCND2
9 0.790 0.080 12 4296223 intron variant A/G snv 0.35 0.700 1.000 1 2013 2013