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rs2237886

From SNPedia

Orientationplus
Stabilizedplus
Make rs2237886(C;C)
Make rs2237886(C;T)
Make rs2237886(T;T)
ReferenceGRCh38 38.1/141
Chromosome11
Position2789501
GeneKCNQ1
is asnp
is mentioned by
dbSNPrs2237886
dbSNP (classic)rs2237886
ClinGenrs2237886
ebirs2237886
HLIrs2237886
Exacrs2237886
Gnomadrs2237886
Varsomers2237886
LitVarrs2237886
Maprs2237886
PheGenIrs2237886
Biobankrs2237886
1000 genomesrs2237886
hgdprs2237886
ensemblrs2237886
geneviewrs2237886
scholarrs2237886
googlers2237886
pharmgkbrs2237886
gwascentralrs2237886
openSNPrs2237886
23andMers2237886
SNPshotrs2237886
SNPdbers2237886
MSV3drs2237886
GWAS Ctlgrs2237886
GMAF0.1198
Max Magnitude0
? (C;C) (C;T) (T;T) 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 T
P-val 2E-13
Odds Ratio 0.0500 [NR] meters increase