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rs121913673

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs121913673(C;G)
Make rs121913673(G;G)
ReferenceGRCh38 38.1/141
Chromosome7
Position116782048
GeneMET
is asnp
is mentioned by
dbSNPrs121913673
ebirs121913673
HLIrs121913673
Exacrs121913673
Varsomers121913673
Maprs121913673
PheGenIrs121913673
hapmaprs121913673
1000 genomesrs121913673
hgdprs121913673
ensemblrs121913673
gopubmedrs121913673
geneviewrs121913673
scholarrs121913673
googlers121913673
pharmgkbrs121913673
gwascentralrs121913673
openSNPrs121913673
23andMers121913673
23andMe allrs121913673
SNP Nexus

SNPshotrs121913673
SNPdbers121913673
MSV3drs121913673
GWAS Ctlgrs121913673
Merged fromRs28932778
Max Magnitude0
OMIM164860
Desc
Variant0006
Relatedalso
ClinVar
Risk rs121913673(G;G)
Alt rs121913673(G;G)
Reference rs121913673(C;C)
Significance Pathogenic
Disease Renal cell carcinoma
Variation info
Gene MET
CLNDBN Renal cell carcinoma, papillary, 1
Reversed 0
HGVS NC_000007.13:g.116422102C>G; NC_000007.13:g.116422102C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000014900.4, RCV000236718.1,