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rs33966734

From SNPedia

Orientationminus
Stabilizedminus
Make rs33966734(G;G)
Make rs33966734(G;T)
Make rs33966734(T;T)
ReferenceGRCh38.p7 38.3/149
Chromosome6
Position41936060
GeneCCND3
is asnp
is mentioned by
dbSNPrs33966734
dbSNP (classic)rs33966734
ClinGenrs33966734
ebirs33966734
HLIrs33966734
Exacrs33966734
Gnomadrs33966734
Varsomers33966734
LitVarrs33966734
Maprs33966734
PheGenIrs33966734
Biobankrs33966734
1000 genomesrs33966734
hgdprs33966734
ensemblrs33966734
geneviewrs33966734
scholarrs33966734
googlers33966734
pharmgkbrs33966734
gwascentralrs33966734
openSNPrs33966734
23andMers33966734
23andMe allrs33966734
SNPshotrs33966734
SNPdbers33966734
MSV3drs33966734
GWAS Ctlgrs33966734
Max Magnitude0

[PMID 28146470OA-icon.png] Rare and low-frequency coding variants alter human adult height.