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rs9844666

From SNPedia

Orientationplus
Stabilizedplus
Make rs9844666(A;A)
Make rs9844666(A;G)
Make rs9844666(G;G)
ReferenceGRCh38 38.1/141
Chromosome3
Position136255374
GenePCCB
is asnp
is mentioned by
dbSNPrs9844666
ebirs9844666
HLIrs9844666
Exacrs9844666
Varsomers9844666
Maprs9844666
PheGenIrs9844666
hapmaprs9844666
1000 genomesrs9844666
hgdprs9844666
ensemblrs9844666
gopubmedrs9844666
geneviewrs9844666
scholarrs9844666
googlers9844666
pharmgkbrs9844666
gwascentralrs9844666
openSNPrs9844666
23andMers9844666
23andMe allrs9844666
SNP Nexus

SNPshotrs9844666
SNPdbers9844666
MSV3drs9844666
GWAS Ctlgrs9844666
GMAF0.09183
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 4E-9
Odds Ratio .02 [NR] unit decrease