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rs121913245

From SNPedia
Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs121913245(C;C)
Make rs121913245(C;T)
ReferenceGRCh38.p7 38.3/150
Chromosome7
Position116783420
GeneMET
is asnp
is mentioned by
dbSNPrs121913245
dbSNP (old)rs121913245
ClinGenrs121913245
ebirs121913245
HLIrs121913245
Exacrs121913245
Gnomadrs121913245
Varsomers121913245
Maprs121913245
PheGenIrs121913245
Biobankrs121913245
1000 genomesrs121913245
hgdprs121913245
ensemblrs121913245
gopubmedrs121913245
geneviewrs121913245
scholarrs121913245
googlers121913245
pharmgkbrs121913245
gwascentralrs121913245
openSNPrs121913245
23andMers121913245
23andMe allrs121913245
SNPshotrs121913245
SNPdbers121913245
MSV3drs121913245
GWAS Ctlgrs121913245
Max Magnitude0
ClinVar
Risk rs121913245(C;C)
Alt rs121913245(C;C)
Reference Rs121913245(T;T)
Significance Probable-Pathogenic
Disease Kidney Carcinoma Carcinoma
Variation info
Gene MET
CLNDBN Kidney Carcinoma Carcinoma
Reversed 0
HGVS NC_000007.13:g.116423474T>C
CLNSRC
CLNACC RCV000425451.1, RCV000442904.1,