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rs2580816

From SNPedia

Orientationplus
Stabilizedplus
Make rs2580816(C;C)
Make rs2580816(C;T)
Make rs2580816(T;T)
ReferenceGRCh38 38.1/141
Chromosome2
Position231933256
is asnp
is mentioned by
dbSNPrs2580816
ebirs2580816
HLIrs2580816
Exacrs2580816
Varsomers2580816
Maprs2580816
PheGenIrs2580816
hapmaprs2580816
1000 genomesrs2580816
hgdprs2580816
ensemblrs2580816
gopubmedrs2580816
geneviewrs2580816
scholarrs2580816
googlers2580816
pharmgkbrs2580816
gwascentralrs2580816
openSNPrs2580816
23andMers2580816
23andMe allrs2580816
SNP Nexus

SNPshotrs2580816
SNPdbers2580816
MSV3drs2580816
GWAS Ctlgrs2580816
GMAF0.3742
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 6E-22
Odds Ratio 0.05 [NR] unit decrease