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rs5757949

From SNPedia

Orientationplus
Stabilizedplus
Make rs5757949(C;C)
Make rs5757949(C;T)
Make rs5757949(T;T)
ReferenceGRCh38 38.1/141
Chromosome22
Position40424147
GeneMKL1
is asnp
is mentioned by
dbSNPrs5757949
ebirs5757949
HLIrs5757949
Exacrs5757949
Varsomers5757949
Maprs5757949
PheGenIrs5757949
hapmaprs5757949
1000 genomesrs5757949
hgdprs5757949
ensemblrs5757949
gopubmedrs5757949
geneviewrs5757949
scholarrs5757949
googlers5757949
pharmgkbrs5757949
gwascentralrs5757949
openSNPrs5757949
23andMers5757949
23andMe allrs5757949
SNP Nexus

SNPshotrs5757949
SNPdbers5757949
MSV3drs5757949
GWAS Ctlgrs5757949
GMAF0.2388
Max Magnitude
? (C;C) (C;T) (T;T) 28
GWAS snp
PMID [PMID 19570815OA-icon.png]
Trait Height
Title A genome-wide association study of northwestern Europeans involves the CNP signaling pathway in the etiology of human height variation
Risk Allele T
P-val 0.000004
Odds Ratio NR NR


GET Evidence
rs5757949
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.203125
summary