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rs121913243

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs121913243(A;G)
Make rs121913243(G;G)
ReferenceGRCh38 38.1/141
Chromosome7
Position116777410
GeneMET
is asnp
is mentioned by
dbSNPrs121913243
ebirs121913243
HLIrs121913243
Exacrs121913243
Varsomers121913243
Maprs121913243
PheGenIrs121913243
hapmaprs121913243
1000 genomesrs121913243
hgdprs121913243
ensemblrs121913243
gopubmedrs121913243
geneviewrs121913243
scholarrs121913243
googlers121913243
pharmgkbrs121913243
gwascentralrs121913243
openSNPrs121913243
23andMers121913243
23andMe allrs121913243
SNP Nexus

SNPshotrs121913243
SNPdbers121913243
MSV3drs121913243
GWAS Ctlgrs121913243
Max Magnitude0
OMIM164860
Desc
Variant0007
Relatedalso
ClinVar
Risk rs121913243(C,G;C,G)
Alt rs121913243(C,G;C,G)
Reference rs121913243(A;A)
Significance Pathogenic
Disease Renal cell carcinoma not provided
Variation info
Gene MET
CLNDBN Renal cell carcinoma, papillary, 1 not provided
Reversed 0
HGVS NC_000007.13:g.116417464A>G
CLNSRC HGMD OMIM Allelic Variant
CLNACC RCV000014901.26, RCV000079490.4,