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

rs4601530

From SNPedia

Orientationplus
Stabilizedplus
Make rs4601530(C;C)
Make rs4601530(C;T)
Make rs4601530(T;T)
ReferenceGRCh38 38.1/141
Chromosome1
Position24717620
is asnp
is mentioned by
dbSNPrs4601530
ebirs4601530
HLIrs4601530
Exacrs4601530
Varsomers4601530
Maprs4601530
PheGenIrs4601530
hapmaprs4601530
1000 genomesrs4601530
hgdprs4601530
ensemblrs4601530
gopubmedrs4601530
geneviewrs4601530
scholarrs4601530
googlers4601530
pharmgkbrs4601530
gwascentralrs4601530
openSNPrs4601530
23andMers4601530
23andMe allrs4601530
SNP Nexus

SNPshotrs4601530
SNPdbers4601530
MSV3drs4601530
GWAS Ctlgrs4601530
GMAF0.3613
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 2E-12
Odds Ratio 0.0300 [NR] meters decrease