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rs121913247

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs121913247(C;C)
Make rs121913247(C;T)
ReferenceGRCh38.p7 38.3/150
Chromosome7
Position116783359
GeneMET
is asnp
is mentioned by
dbSNPrs121913247
dbSNP (old)rs121913247
ClinGenrs121913247
ebirs121913247
HLIrs121913247
Exacrs121913247
Gnomadrs121913247
Varsomers121913247
Maprs121913247
PheGenIrs121913247
Biobankrs121913247
1000 genomesrs121913247
hgdprs121913247
ensemblrs121913247
gopubmedrs121913247
geneviewrs121913247
scholarrs121913247
googlers121913247
pharmgkbrs121913247
gwascentralrs121913247
openSNPrs121913247
23andMers121913247
23andMe allrs121913247
SNPshotrs121913247
SNPdbers121913247
MSV3drs121913247
GWAS Ctlgrs121913247
Max Magnitude0
ClinVar
Risk rs121913247(C;C)
Alt rs121913247(C;C)
Reference Rs121913247(T;T)
Significance Probable-Pathogenic
Disease not specified Kidney Carcinoma Carcinoma
Variation info
Gene MET
CLNDBN not specified Kidney Carcinoma Carcinoma
Reversed 0
HGVS NC_000007.13:g.116423413T>C
CLNSRC
CLNACC RCV000175410.1, RCV000417458.1, RCV000431224.1,