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rs121913675

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs121913675(C;T)
Make rs121913675(T;T)
ReferenceGRCh38 38.1/141
Chromosome7
Position116778953
GeneMET
is asnp
is mentioned by
dbSNPrs121913675
ebirs121913675
HLIrs121913675
Exacrs121913675
Varsomers121913675
Maprs121913675
PheGenIrs121913675
hapmaprs121913675
1000 genomesrs121913675
hgdprs121913675
ensemblrs121913675
gopubmedrs121913675
geneviewrs121913675
scholarrs121913675
googlers121913675
pharmgkbrs121913675
gwascentralrs121913675
openSNPrs121913675
23andMers121913675
23andMe allrs121913675
SNP Nexus

SNPshotrs121913675
SNPdbers121913675
MSV3drs121913675
GWAS Ctlgrs121913675
Max Magnitude0
OMIM164860
Desc
Variant0008
Relatedalso
ClinVar
Risk rs121913675(T;T)
Alt rs121913675(T;T)
Reference rs121913675(C;C)
Significance Pathogenic
Disease Childhood hepatocellular carcinoma
Variation info
Gene MET
CLNDBN Childhood hepatocellular carcinoma
Reversed 0
HGVS NC_000007.13:g.116419007C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000014902.6,