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rs7652177

From SNPedia

Orientationplus
Stabilizedplus
Make rs7652177(C;C)
Make rs7652177(C;G)
Make rs7652177(G;G)
ReferenceGRCh38 38.1/141
Chromosome3
Position172251287
GeneFNDC3B
is asnp
is mentioned by
dbSNPrs7652177
ebirs7652177
HLIrs7652177
Exacrs7652177
Varsomers7652177
Maprs7652177
PheGenIrs7652177
hapmaprs7652177
1000 genomesrs7652177
hgdprs7652177
ensemblrs7652177
gopubmedrs7652177
geneviewrs7652177
scholarrs7652177
googlers7652177
pharmgkbrs7652177
gwascentralrs7652177
openSNPrs7652177
23andMers7652177
23andMe allrs7652177
SNP Nexus

SNPshotrs7652177
SNPdbers7652177
MSV3drs7652177
GWAS Ctlgrs7652177
GMAF0.3884
Max Magnitude
? (C;C) (C;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
P-val 7E-11
Odds Ratio NR NR