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rs121913670

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs121913670(A;A)
Make rs121913670(A;G)
ReferenceGRCh38 38.1/141
Chromosome7
Position116783329
GeneMET
is asnp
is mentioned by
dbSNPrs121913670
ebirs121913670
HLIrs121913670
Exacrs121913670
Varsomers121913670
Maprs121913670
PheGenIrs121913670
hapmaprs121913670
1000 genomesrs121913670
hgdprs121913670
ensemblrs121913670
gopubmedrs121913670
geneviewrs121913670
scholarrs121913670
googlers121913670
pharmgkbrs121913670
gwascentralrs121913670
openSNPrs121913670
23andMers121913670
23andMe allrs121913670
SNP Nexus

SNPshotrs121913670
SNPdbers121913670
MSV3drs121913670
GWAS Ctlgrs121913670
Merged fromRs28932776
Max Magnitude0
OMIM164860
Desc
Variant0003
Relatedalso
ClinVar
Risk rs121913670(A;A)
Alt rs121913670(A;A)
Reference rs121913670(G;G)
Significance Pathogenic
Disease Renal cell carcinoma Tumor susceptibility linked to germline BAP1 mutations
Variation info
Gene MET
CLNDBN Renal cell carcinoma, papillary, 1 Tumor susceptibility linked to germline BAP1 mutations
Reversed 0
HGVS NC_000007.13:g.116423383G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000014897.25, RCV000221989.1,