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rs10243024

From SNPedia

Orientationplus
Stabilizedplus
Make rs10243024(A;A)
Make rs10243024(A;G)
Make rs10243024(G;G)
ReferenceGRCh38 38.1/141
Chromosome7
Position116706549
GeneMET
is asnp
is mentioned by
dbSNPrs10243024
ebirs10243024
HLIrs10243024
Exacrs10243024
Varsomers10243024
Maprs10243024
PheGenIrs10243024
hapmaprs10243024
1000 genomesrs10243024
hgdprs10243024
ensemblrs10243024
gopubmedrs10243024
geneviewrs10243024
scholarrs10243024
googlers10243024
pharmgkbrs10243024
gwascentralrs10243024
openSNPrs10243024
23andMers10243024
23andMe allrs10243024
SNP Nexus

SNPshotrs10243024
SNPdbers10243024
MSV3drs10243024
GWAS Ctlgrs10243024
GMAF0.3177
Max Magnitude
? (A;A) (A;G) (G;G) 28
GWAS snp
PMID [PMID 19010793OA-icon.png]
Trait Multiple sclerosis (severity)
Title Genome-wide association analysis of susceptibility and clinical phenotype in multiple sclerosis
Risk Allele
P-val 0.000006
Odds Ratio NR NR



[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.


GET Evidence
rs10243024
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.359375
summary