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: rs10947997
rs10947997
CCND3
4 6 41953503 intron variant G/T snv 0.13 0.700 1.000 1 2016 2016
dbSNP: rs113267280
rs113267280
CCND3
1 6 41984773 intron variant T/G snv 7.3E-03 0.700 1.000 1 2016 2016
dbSNP: rs9349205
rs9349205
CCND3
7 6 41957421 intron variant G/A;C snv 0.700 1.000 1 2016 2016