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rs17480616

From SNPedia

Orientationplus
Stabilizedplus
Make rs17480616(C;C)
Make rs17480616(C;G)
Make rs17480616(G;G)
ReferenceGRCh38.p7 38.3/149
Chromosome7
Position135438312
GeneCNOT4
is asnp
is mentioned by
dbSNPrs17480616
dbSNP (old)rs17480616
ClinGenrs17480616
ebirs17480616
HLIrs17480616
Exacrs17480616
Gnomadrs17480616
Varsomers17480616
LitVarrs17480616
Maprs17480616
PheGenIrs17480616
Biobankrs17480616
1000 genomesrs17480616
hgdprs17480616
ensemblrs17480616
gopubmedrs17480616
geneviewrs17480616
scholarrs17480616
googlers17480616
pharmgkbrs17480616
gwascentralrs17480616
openSNPrs17480616
23andMers17480616
23andMe allrs17480616
SNPshotrs17480616
SNPdbers17480616
MSV3drs17480616
GWAS Ctlgrs17480616
Max Magnitude
? (C;C) (C;G) (G;G) 28

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