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rs11118346

From SNPedia

Orientationplus
Stabilizedplus
Make rs11118346(C;C)
Make rs11118346(C;T)
Make rs11118346(T;T)
ReferenceGRCh38 38.1/141
Chromosome1
Position219570377
is asnp
is mentioned by
dbSNPrs11118346
ebirs11118346
HLIrs11118346
Exacrs11118346
Varsomers11118346
Maprs11118346
PheGenIrs11118346
hapmaprs11118346
1000 genomesrs11118346
hgdprs11118346
ensemblrs11118346
gopubmedrs11118346
geneviewrs11118346
scholarrs11118346
googlers11118346
pharmgkbrs11118346
gwascentralrs11118346
openSNPrs11118346
23andMers11118346
23andMe allrs11118346
SNP Nexus

SNPshotrs11118346
SNPdbers11118346
MSV3drs11118346
GWAS Ctlgrs11118346
GMAF0.4073
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 2E-12
Odds Ratio .03 [NR] unit decrease