Have questions? Visit https://www.reddit.com/r/SNPedia

rs1814175

From SNPedia

Orientationplus
Stabilizedplus
Make rs1814175(C;C)
Make rs1814175(C;T)
Make rs1814175(T;T)
ReferenceGRCh38 38.1/141
Chromosome11
Position49537620
is asnp
is mentioned by
dbSNPrs1814175
ebirs1814175
HLIrs1814175
Exacrs1814175
Varsomers1814175
Maprs1814175
PheGenIrs1814175
hapmaprs1814175
1000 genomesrs1814175
hgdprs1814175
ensemblrs1814175
gopubmedrs1814175
geneviewrs1814175
scholarrs1814175
googlers1814175
pharmgkbrs1814175
gwascentralrs1814175
openSNPrs1814175
23andMers1814175
23andMe allrs1814175
SNP Nexus

SNPshotrs1814175
SNPdbers1814175
MSV3drs1814175
GWAS Ctlgrs1814175
GMAF0.4844
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-8
Odds Ratio .02 [NR] unit increase