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rs4470914

From SNPedia

Orientationplus
Stabilizedplus
Make rs4470914(C;C)
Make rs4470914(C;T)
Make rs4470914(T;T)
ReferenceGRCh38 38.1/141
Chromosome7
Position19576899
is asnp
is mentioned by
dbSNPrs4470914
ebirs4470914
HLIrs4470914
Exacrs4470914
Varsomers4470914
Maprs4470914
PheGenIrs4470914
hapmaprs4470914
1000 genomesrs4470914
hgdprs4470914
ensemblrs4470914
gopubmedrs4470914
geneviewrs4470914
scholarrs4470914
googlers4470914
pharmgkbrs4470914
gwascentralrs4470914
openSNPrs4470914
23andMers4470914
23andMe allrs4470914
SNP Nexus

SNPshotrs4470914
SNPdbers4470914
MSV3drs4470914
GWAS Ctlgrs4470914
GMAF0.2264
Max Magnitude
? (C;C) (C;T) (T;T) 28
GWAS snp
PMID [PMID 20881960OA-icon.png]
Trait
Title Hundreds of variants clustered in genomic loci and biological pathways affect human height.
Risk Allele T
P-val 9E-10
Odds Ratio 0.0300 [NR] meters decrease