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

rs1582931

From SNPedia

Orientationminus
Stabilizedminus
Make rs1582931(C;C)
Make rs1582931(C;T)
Make rs1582931(T;T)
ReferenceGRCh38 38.1/141
Chromosome5
Position123321505
is asnp
is mentioned by
dbSNPrs1582931
ebirs1582931
HLIrs1582931
Exacrs1582931
Varsomers1582931
Maprs1582931
PheGenIrs1582931
hapmaprs1582931
1000 genomesrs1582931
hgdprs1582931
ensemblrs1582931
gopubmedrs1582931
geneviewrs1582931
scholarrs1582931
googlers1582931
pharmgkbrs1582931
gwascentralrs1582931
openSNPrs1582931
23andMers1582931
23andMe allrs1582931
SNP Nexus

SNPshotrs1582931
SNPdbers1582931
MSV3drs1582931
GWAS Ctlgrs1582931
GMAF0.4412
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 A
P-val 2E-10
Odds Ratio 0.0200 [NR] meters decrease