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rs2597513

From SNPedia

Orientationplus
Stabilizedplus
Make rs2597513(C;C)
Make rs2597513(C;T)
Make rs2597513(T;T)
ReferenceGRCh38 38.1/141
Chromosome3
Position13514336
is asnp
is mentioned by
dbSNPrs2597513
dbSNP (old)rs2597513
ClinGenrs2597513
ebirs2597513
HLIrs2597513
Exacrs2597513
Gnomadrs2597513
Varsomers2597513
Maprs2597513
PheGenIrs2597513
Biobankrs2597513
1000 genomesrs2597513
hgdprs2597513
ensemblrs2597513
gopubmedrs2597513
geneviewrs2597513
scholarrs2597513
googlers2597513
pharmgkbrs2597513
gwascentralrs2597513
openSNPrs2597513
23andMers2597513
23andMe allrs2597513
SNP Nexus

SNPshotrs2597513
SNPdbers2597513
MSV3drs2597513
GWAS Ctlgrs2597513
GMAF0.09137
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 7E-10
Odds Ratio 0.0400 [NR] meters decrease