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rs2629046

From SNPedia

Orientationplus
Stabilizedplus
Make rs2629046(C;C)
Make rs2629046(C;T)
Make rs2629046(T;T)
ReferenceGRCh38 38.1/141
Chromosome2
Position224183027
is asnp
is mentioned by
dbSNPrs2629046
ebirs2629046
HLIrs2629046
Exacrs2629046
Varsomers2629046
Maprs2629046
PheGenIrs2629046
hapmaprs2629046
1000 genomesrs2629046
hgdprs2629046
ensemblrs2629046
gopubmedrs2629046
geneviewrs2629046
scholarrs2629046
googlers2629046
pharmgkbrs2629046
gwascentralrs2629046
openSNPrs2629046
23andMers2629046
23andMe allrs2629046
SNP Nexus

SNPshotrs2629046
SNPdbers2629046
MSV3drs2629046
GWAS Ctlgrs2629046
GMAF0.4582
Max Magnitude
? (C;C) (C;T) (T;T) 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 T
P-val 8E-12
Odds Ratio .02 [NR] unit increase