Have questions? Visit https://www.reddit.com/r/SNPedia

rs121913676

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs121913676(A;A)
Make rs121913676(A;G)
ReferenceGRCh38 38.1/141
Chromosome7
Position116783421
GeneMET
is asnp
is mentioned by
dbSNPrs121913676
ebirs121913676
HLIrs121913676
Exacrs121913676
Varsomers121913676
Maprs121913676
PheGenIrs121913676
hapmaprs121913676
1000 genomesrs121913676
hgdprs121913676
ensemblrs121913676
gopubmedrs121913676
geneviewrs121913676
scholarrs121913676
googlers121913676
pharmgkbrs121913676
gwascentralrs121913676
openSNPrs121913676
23andMers121913676
23andMe allrs121913676
SNP Nexus

SNPshotrs121913676
SNPdbers121913676
MSV3drs121913676
GWAS Ctlgrs121913676
Max Magnitude0
OMIM164860
Desc
Variant0009
Relatedalso
ClinVar
Risk rs121913676(A;A)
Alt rs121913676(A;A)
Reference rs121913676(G;G)
Significance Pathogenic
Disease Childhood hepatocellular carcinoma
Variation info
Gene MET
CLNDBN Childhood hepatocellular carcinoma
Reversed 0
HGVS NC_000007.13:g.116423475G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000014903.6,