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rs2341459

From SNPedia

Orientationplus
Stabilizedplus
Make rs2341459(C;C)
Make rs2341459(C;T)
Make rs2341459(T;T)
ReferenceGRCh38 38.1/141
Chromosome2
Position44541063
GeneCAMKMT
is asnp
is mentioned by
dbSNPrs2341459
ClinGenrs2341459
ebirs2341459
HLIrs2341459
Exacrs2341459
Varsomers2341459
Maprs2341459
PheGenIrs2341459
hapmaprs2341459
1000 genomesrs2341459
hgdprs2341459
ensemblrs2341459
gopubmedrs2341459
geneviewrs2341459
scholarrs2341459
googlers2341459
pharmgkbrs2341459
gwascentralrs2341459
openSNPrs2341459
23andMers2341459
23andMe allrs2341459
SNP Nexus

SNPshotrs2341459
SNPdbers2341459
MSV3drs2341459
GWAS Ctlgrs2341459
GMAF0.3852
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-10
Odds Ratio .03 [NR] unit increase