Have data from 23andMe or Ancestry? Make a report automatically with Promethease !

rs121913244

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs121913244(C;T)
Make rs121913244(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome7
Position116777409
GeneMET
is asnp
is mentioned by
dbSNPrs121913244
dbSNP (old)rs121913244
ClinGenrs121913244
ebirs121913244
HLIrs121913244
Exacrs121913244
Gnomadrs121913244
Varsomers121913244
Maprs121913244
PheGenIrs121913244
Biobankrs121913244
1000 genomesrs121913244
hgdprs121913244
ensemblrs121913244
gopubmedrs121913244
geneviewrs121913244
scholarrs121913244
googlers121913244
pharmgkbrs121913244
gwascentralrs121913244
openSNPrs121913244
23andMers121913244
23andMe allrs121913244
SNPshotrs121913244
SNPdbers121913244
MSV3drs121913244
GWAS Ctlgrs121913244
Max Magnitude0
ClinVar
Risk rs121913244(T;T)
Alt rs121913244(T;T)
Reference Rs121913244(C;C)
Significance Probable-Pathogenic
Disease Kidney Carcinoma
Variation info
Gene MET
CLNDBN Kidney Carcinoma
Reversed 0
HGVS NC_000007.13:g.116417463C>T
CLNSRC
CLNACC RCV000435140.1,