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rs2780226

From SNPedia

Orientationminus
Stabilizedminus
Make rs2780226(A;A)
Make rs2780226(A;G)
Make rs2780226(G;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position34231315
is asnp
is mentioned by
dbSNPrs2780226
dbSNP (classic)rs2780226
ClinGenrs2780226
ebirs2780226
HLIrs2780226
Exacrs2780226
Gnomadrs2780226
Varsomers2780226
LitVarrs2780226
Maprs2780226
PheGenIrs2780226
Biobankrs2780226
1000 genomesrs2780226
hgdprs2780226
ensemblrs2780226
geneviewrs2780226
scholarrs2780226
googlers2780226
pharmgkbrs2780226
gwascentralrs2780226
openSNPrs2780226
23andMers2780226
SNPshotrs2780226
SNPdbers2780226
MSV3drs2780226
GWAS Ctlgrs2780226
GMAF0.2126
Max Magnitude0
? (A;A) (A;G) (G;G) 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 8E-28
Odds Ratio .08 [NR] unit decrease