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rs121913677

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs121913677(A;G)
Make rs121913677(G;G)
ReferenceGRCh38 38.1/141
Chromosome7
Position116783402
GeneMET
is asnp
is mentioned by
dbSNPrs121913677
ebirs121913677
HLIrs121913677
Exacrs121913677
Varsomers121913677
Maprs121913677
PheGenIrs121913677
hapmaprs121913677
1000 genomesrs121913677
hgdprs121913677
ensemblrs121913677
gopubmedrs121913677
geneviewrs121913677
scholarrs121913677
googlers121913677
pharmgkbrs121913677
gwascentralrs121913677
openSNPrs121913677
23andMers121913677
23andMe allrs121913677
SNP Nexus

SNPshotrs121913677
SNPdbers121913677
MSV3drs121913677
GWAS Ctlgrs121913677
Max Magnitude0
OMIM164860
Desc
Variant0010
Relatedalso
ClinVar
Risk rs121913677(G;G)
Alt rs121913677(G;G)
Reference rs121913677(A;A)
Significance Pathogenic
Disease Childhood hepatocellular carcinoma
Variation info
Gene MET
CLNDBN Childhood hepatocellular carcinoma
Reversed 0
HGVS NC_000007.13:g.116423456A>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000014904.6,