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rs7460090

From SNPedia

Orientationplus
Stabilizedplus
Make rs7460090(C;C)
Make rs7460090(C;T)
Make rs7460090(T;T)
ReferenceGRCh38 38.1/141
Chromosome8
Position56281604
is asnp
is mentioned by
dbSNPrs7460090
ebirs7460090
HLIrs7460090
Exacrs7460090
Varsomers7460090
Maprs7460090
PheGenIrs7460090
hapmaprs7460090
1000 genomesrs7460090
hgdprs7460090
ensemblrs7460090
gopubmedrs7460090
geneviewrs7460090
scholarrs7460090
googlers7460090
pharmgkbrs7460090
gwascentralrs7460090
openSNPrs7460090
23andMers7460090
23andMe allrs7460090
SNP Nexus

SNPshotrs7460090
SNPdbers7460090
MSV3drs7460090
GWAS Ctlgrs7460090
GMAF0.1221
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 8E-27
Odds Ratio .06 [NR] unit increase


[PMID 20027299OA-icon.png] Transferability and fine-mapping of genome-wide associated loci for adult height across human populations.