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rs1367226

From SNPedia

Orientationminus
Stabilizedminus
Make rs1367226(C;C)
Make rs1367226(C;T)
Make rs1367226(T;T)
ReferenceGRCh38 38.1/141
Chromosome2
Position55862405
is asnp
is mentioned by
dbSNPrs1367226
ebirs1367226
HLIrs1367226
Exacrs1367226
Varsomers1367226
Maprs1367226
PheGenIrs1367226
hapmaprs1367226
1000 genomesrs1367226
hgdprs1367226
ensemblrs1367226
gopubmedrs1367226
geneviewrs1367226
scholarrs1367226
googlers1367226
pharmgkbrs1367226
gwascentralrs1367226
openSNPrs1367226
23andMers1367226
23andMe allrs1367226
SNP Nexus

SNPshotrs1367226
SNPdbers1367226
MSV3drs1367226
GWAS Ctlgrs1367226
GMAF0.2801
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
P-val 4E-8
Odds Ratio NR NR