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rs10037512

From SNPedia

Orientationplus
Stabilizedplus
Make rs10037512(C;C)
Make rs10037512(C;T)
Make rs10037512(T;T)
ReferenceGRCh38 38.1/141
Chromosome5
Position89058858
is asnp
is mentioned by
dbSNPrs10037512
ebirs10037512
HLIrs10037512
Exacrs10037512
Varsomers10037512
Maprs10037512
PheGenIrs10037512
hapmaprs10037512
1000 genomesrs10037512
hgdprs10037512
ensemblrs10037512
gopubmedrs10037512
geneviewrs10037512
scholarrs10037512
googlers10037512
pharmgkbrs10037512
gwascentralrs10037512
openSNPrs10037512
23andMers10037512
23andMe allrs10037512
SNP Nexus

SNPshotrs10037512
SNPdbers10037512
MSV3drs10037512
GWAS Ctlgrs10037512
GMAF0.3783
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 2E-18
Odds Ratio 0.03 [NR] unit increase