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rs822552

From SNPedia

Orientationplus
Stabilizedplus
Make rs822552(C;C)
Make rs822552(C;G)
Make rs822552(G;G)
ReferenceGRCh38 38.1/141
Chromosome7
Position148953542
is asnp
is mentioned by
dbSNPrs822552
ebirs822552
HLIrs822552
Exacrs822552
Varsomers822552
Maprs822552
PheGenIrs822552
hapmaprs822552
1000 genomesrs822552
hgdprs822552
ensemblrs822552
gopubmedrs822552
geneviewrs822552
scholarrs822552
googlers822552
pharmgkbrs822552
gwascentralrs822552
openSNPrs822552
23andMers822552
23andMe allrs822552
SNP Nexus

SNPshotrs822552
SNPdbers822552
MSV3drs822552
GWAS Ctlgrs822552
GMAF0.2796
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 C
P-val 3E-8
Odds Ratio .03 [NR] unit decrease