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rs3118905

From SNPedia

Orientationplus
Stabilizedplus
Make rs3118905(A;A)
Make rs3118905(A;G)
Make rs3118905(G;G)
ReferenceGRCh38 38.1/141
Chromosome13
Position50531198
is asnp
is mentioned by
dbSNPrs3118905
ebirs3118905
HLIrs3118905
Exacrs3118905
Varsomers3118905
Maprs3118905
PheGenIrs3118905
hapmaprs3118905
1000 genomesrs3118905
hgdprs3118905
ensemblrs3118905
gopubmedrs3118905
geneviewrs3118905
scholarrs3118905
googlers3118905
pharmgkbrs3118905
gwascentralrs3118905
openSNPrs3118905
23andMers3118905
23andMe allrs3118905
SNP Nexus

SNPshotrs3118905
SNPdbers3118905
MSV3drs3118905
GWAS Ctlgrs3118905
GMAF0.1556
Max Magnitude
? (A;A) (A;G) (G;G) 28
GWAS snp
PMID [PMID 20881960OA-icon.png]
Trait Height
Title Hundreds of variants clustered in genomic loci and biological pathways affect human height.
Risk Allele A
P-val 1E-45
Odds Ratio .06 [NR] unit decrease


[PMID 19570815OA-icon.png] A genome-wide association study of northwestern Europeans involves the C-type natriuretic peptide signaling pathway in the etiology of human height variation.