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rs121913246

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs121913246(A;G)
Make rs121913246(G;G)
ReferenceGRCh38 38.1/141
Chromosome7
Position116783360
GeneMET
is asnp
is mentioned by
dbSNPrs121913246
ebirs121913246
HLIrs121913246
Exacrs121913246
Varsomers121913246
Maprs121913246
PheGenIrs121913246
hapmaprs121913246
1000 genomesrs121913246
hgdprs121913246
ensemblrs121913246
gopubmedrs121913246
geneviewrs121913246
scholarrs121913246
googlers121913246
pharmgkbrs121913246
gwascentralrs121913246
openSNPrs121913246
23andMers121913246
23andMe allrs121913246
SNP Nexus

SNPshotrs121913246
SNPdbers121913246
MSV3drs121913246
GWAS Ctlgrs121913246
Max Magnitude0
OMIM164860
Desc
Variant0005
Relatedalso
ClinVar
Risk rs121913246(G;G)
Alt rs121913246(G;G)
Reference rs121913246(A;A)
Significance Pathogenic
Disease Renal cell carcinoma
Variation info
Gene MET
CLNDBN Renal cell carcinoma, papillary, 1
Reversed 0
HGVS NC_000007.13:g.116423414A>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000014899.21,