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rs10152591

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common on affy axiom data
Make rs10152591(A;C)
Make rs10152591(C;C)
ReferenceGRCh38 38.1/141
Chromosome15
Position69755818
is asnp
is mentioned by
dbSNPrs10152591
ebirs10152591
HLIrs10152591
Exacrs10152591
Varsomers10152591
Maprs10152591
PheGenIrs10152591
hapmaprs10152591
1000 genomesrs10152591
hgdprs10152591
ensemblrs10152591
gopubmedrs10152591
geneviewrs10152591
scholarrs10152591
googlers10152591
pharmgkbrs10152591
gwascentralrs10152591
openSNPrs10152591
23andMers10152591
23andMe allrs10152591
SNP Nexus

SNPshotrs10152591
SNPdbers10152591
MSV3drs10152591
GWAS Ctlgrs10152591
GMAF0.0629
Max Magnitude0
? (A;A) (A;C) (C;C) 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 3E-10
Odds Ratio 0.0400 [NR] meters increase