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rs4821083

From SNPedia

Orientationplus
Stabilizedplus
Make rs4821083(C;C)
Make rs4821083(C;T)
Make rs4821083(T;T)
ReferenceGRCh38 38.1/141
Chromosome22
Position32660355
GeneSYN3
is asnp
is mentioned by
dbSNPrs4821083
ebirs4821083
HLIrs4821083
Exacrs4821083
Varsomers4821083
Maprs4821083
PheGenIrs4821083
hapmaprs4821083
1000 genomesrs4821083
hgdprs4821083
ensemblrs4821083
gopubmedrs4821083
geneviewrs4821083
scholarrs4821083
googlers4821083
pharmgkbrs4821083
gwascentralrs4821083
openSNPrs4821083
23andMers4821083
23andMe allrs4821083
SNP Nexus

SNPshotrs4821083
SNPdbers4821083
MSV3drs4821083
GWAS Ctlgrs4821083
Max Magnitude
? (C;C) (C;T) (T;T) 28
GWAS snp
PMID [PMID 20881960OA-icon.png]
Trait
Title Hundreds of variants clustered in genomic loci and biological pathways affect human height.
Risk Allele T
P-val 3E-10
Odds Ratio 0.0300 [NR] meters increase