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rs786202724

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs786202724(A;A)
Make rs786202724(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome7
Position116777403
GeneMET
is asnp
is mentioned by
dbSNPrs786202724
ebirs786202724
HLIrs786202724
Exacrs786202724
Varsomers786202724
Maprs786202724
PheGenIrs786202724
hapmaprs786202724
1000 genomesrs786202724
hgdprs786202724
ensemblrs786202724
gopubmedrs786202724
geneviewrs786202724
scholarrs786202724
googlers786202724
pharmgkbrs786202724
gwascentralrs786202724
openSNPrs786202724
23andMers786202724
23andMe allrs786202724
SNP Nexus

SNPshotrs786202724
SNPdbers786202724
MSV3drs786202724
GWAS Ctlgrs786202724
Max Magnitude0
ClinVar
Risk rs786202724(A;A)
Alt rs786202724(A;A)
Reference rs786202724(G;G)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene MET
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000007.13:g.116417457G>A
CLNSRC
CLNACC RCV000165679.1,