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rs38857

From SNPedia

Orientationplus
Stabilizedplus
Make rs38857(C;C)
Make rs38857(C;T)
Make rs38857(T;T)
ReferenceGRCh38 38.1/141
Chromosome7
Position116725359
GeneMET
is asnp
is mentioned by
dbSNPrs38857
ebirs38857
HLIrs38857
Exacrs38857
Varsomers38857
Maprs38857
PheGenIrs38857
hapmaprs38857
1000 genomesrs38857
hgdprs38857
ensemblrs38857
gopubmedrs38857
geneviewrs38857
scholarrs38857
googlers38857
pharmgkbrs38857
gwascentralrs38857
openSNPrs38857
23andMers38857
23andMe allrs38857
SNP Nexus

SNPshotrs38857
SNPdbers38857
MSV3drs38857
GWAS Ctlgrs38857
GMAF0.2332
Max Magnitude
? (C;C) (C;T) (T;T) 28

[PMID 20416453] c-MET pathway involvement in chronic rhinosinusitis: a genetic association analysis

[PMID 19002214OA-icon.png] MET and autism susceptibility: family and case-control studies.

[PMID 20011629OA-icon.png] The hepatocyte growth factor receptor (MET) gene is not associated with refractive error and ocular biometrics in a Caucasian population.

[PMID 20080979OA-icon.png] Association of genetic variation in the MET proto-oncogene with schizophrenia and general cognitive ability.


[PMID 24766640OA-icon.png] Evaluation of MYOC, ACAN, HGF, and MET as Candidate Genes for High Myopia in a Han Chinese Population