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rs10859563

From SNPedia

Orientationplus
Stabilizedplus
Make rs10859563(C;C)
Make rs10859563(C;G)
Make rs10859563(G;G)
ReferenceGRCh38 38.1/141
Chromosome12
Position93726563
GeneCRADD
is asnp
is mentioned by
dbSNPrs10859563
ebirs10859563
HLIrs10859563
Exacrs10859563
Varsomers10859563
Maprs10859563
PheGenIrs10859563
hapmaprs10859563
1000 genomesrs10859563
hgdprs10859563
ensemblrs10859563
gopubmedrs10859563
geneviewrs10859563
scholarrs10859563
googlers10859563
pharmgkbrs10859563
gwascentralrs10859563
openSNPrs10859563
23andMers10859563
23andMe allrs10859563
SNP Nexus

SNPshotrs10859563
SNPdbers10859563
MSV3drs10859563
GWAS Ctlgrs10859563
GMAF0.4334
Max Magnitude
? (C;C) (C;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
P-val 3E-12
Odds Ratio NR NR