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rs7319045

From SNPedia

Orientationplus
Stabilizedplus
Make rs7319045(A;A)
Make rs7319045(A;G)
Make rs7319045(G;G)
ReferenceGRCh38 38.1/141
Chromosome13
Position91372320
is asnp
is mentioned by
dbSNPrs7319045
ebirs7319045
HLIrs7319045
Exacrs7319045
Varsomers7319045
Maprs7319045
PheGenIrs7319045
hapmaprs7319045
1000 genomesrs7319045
hgdprs7319045
ensemblrs7319045
gopubmedrs7319045
geneviewrs7319045
scholarrs7319045
googlers7319045
pharmgkbrs7319045
gwascentralrs7319045
openSNPrs7319045
23andMers7319045
23andMe allrs7319045
SNP Nexus

SNPshotrs7319045
SNPdbers7319045
MSV3drs7319045
GWAS Ctlgrs7319045
GMAF0.4734
Max Magnitude
? (A;A) (A;G) (G;G) 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 1E-11
Odds Ratio 0.0300 [NR] meters increase