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rs121913671

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs121913671(A;A)
Make rs121913671(A;G)
ReferenceGRCh38 38.1/141
Chromosome7
Position116783353
GeneMET
is asnp
is mentioned by
dbSNPrs121913671
ebirs121913671
HLIrs121913671
Exacrs121913671
Varsomers121913671
Maprs121913671
PheGenIrs121913671
hapmaprs121913671
1000 genomesrs121913671
hgdprs121913671
ensemblrs121913671
gopubmedrs121913671
geneviewrs121913671
scholarrs121913671
googlers121913671
pharmgkbrs121913671
gwascentralrs121913671
openSNPrs121913671
23andMers121913671
23andMe allrs121913671
SNP Nexus

SNPshotrs121913671
SNPdbers121913671
MSV3drs121913671
GWAS Ctlgrs121913671
Merged fromRs28932777
Max Magnitude0
OMIM164860
Desc
Variant0004
Relatedalso
ClinVar
Risk rs121913671(A;A)
Alt rs121913671(A;A)
Reference rs121913671(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.116423407G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000014898.25,