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rs6449353

From SNPedia

Orientationplus
Stabilizedplus
Make rs6449353(C;C)
Make rs6449353(C;T)
Make rs6449353(T;T)
ReferenceGRCh38 38.1/141
Chromosome4
Position18031865
is asnp
is mentioned by
dbSNPrs6449353
ebirs6449353
HLIrs6449353
Exacrs6449353
Varsomers6449353
Maprs6449353
PheGenIrs6449353
hapmaprs6449353
1000 genomesrs6449353
hgdprs6449353
ensemblrs6449353
gopubmedrs6449353
geneviewrs6449353
scholarrs6449353
googlers6449353
pharmgkbrs6449353
gwascentralrs6449353
openSNPrs6449353
23andMers6449353
23andMe allrs6449353
SNP Nexus

SNPshotrs6449353
SNPdbers6449353
MSV3drs6449353
GWAS Ctlgrs6449353
GMAF0.2218
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 7E-46
Odds Ratio .08 [NR] unit increase