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rs121913669

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs121913669(G;T)
Make rs121913669(T;T)
ReferenceGRCh38 38.1/141
Chromosome7
Position116782027
GeneMET
is asnp
is mentioned by
dbSNPrs121913669
ebirs121913669
HLIrs121913669
Exacrs121913669
Varsomers121913669
Maprs121913669
PheGenIrs121913669
hapmaprs121913669
1000 genomesrs121913669
hgdprs121913669
ensemblrs121913669
gopubmedrs121913669
geneviewrs121913669
scholarrs121913669
googlers121913669
pharmgkbrs121913669
gwascentralrs121913669
openSNPrs121913669
23andMers121913669
23andMe allrs121913669
SNP Nexus

SNPshotrs121913669
SNPdbers121913669
MSV3drs121913669
GWAS Ctlgrs121913669
Merged fromRs28932775
Max Magnitude0
OMIM164860
Desc
Variant0002
Relatedalso
ClinVar
Risk rs121913669(A,T;A,T)
Alt rs121913669(A,T;A,T)
Reference rs121913669(G;G)
Significance Pathogenic
Disease Renal cell carcinoma
Variation info
Gene MET
CLNDBN Renal cell carcinoma, papillary, 1
Reversed 0
HGVS NC_000007.13:g.116422081G>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000014896.25,