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rs121913668

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs121913668(C;C)
Make rs121913668(C;T)
ReferenceGRCh38 38.1/141
Chromosome7
Position116778827
GeneMET
is asnp
is mentioned by
dbSNPrs121913668
ebirs121913668
HLIrs121913668
Exacrs121913668
Varsomers121913668
Maprs121913668
PheGenIrs121913668
hapmaprs121913668
1000 genomesrs121913668
hgdprs121913668
ensemblrs121913668
gopubmedrs121913668
geneviewrs121913668
scholarrs121913668
googlers121913668
pharmgkbrs121913668
gwascentralrs121913668
openSNPrs121913668
23andMers121913668
23andMe allrs121913668
SNP Nexus

SNPshotrs121913668
SNPdbers121913668
MSV3drs121913668
GWAS Ctlgrs121913668
Merged fromRs28933101
Max Magnitude0
OMIM164860
Desc
Variant0001
Relatedalso
ClinVar
Risk rs121913668(C;C)
Alt rs121913668(C;C)
Reference rs121913668(T;T)
Significance Pathogenic
Disease Renal cell carcinoma
Variation info
Gene MET
CLNDBN Renal cell carcinoma, papillary, 1
Reversed 0
HGVS NC_000007.13:g.116418881T>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000014895.21,