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rs1057519824

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs1057519824(G;G)
Make rs1057519824(G;T)
ReferenceGRCh38.p7 38.3/150
Chromosome7
Position116783374
GeneMET
is asnp
is mentioned by
dbSNPrs1057519824
dbSNP (classic)rs1057519824
ClinGenrs1057519824
ebirs1057519824
HLIrs1057519824
Exacrs1057519824
Gnomadrs1057519824
Varsomers1057519824
LitVarrs1057519824
Maprs1057519824
PheGenIrs1057519824
Biobankrs1057519824
1000 genomesrs1057519824
hgdprs1057519824
ensemblrs1057519824
geneviewrs1057519824
scholarrs1057519824
googlers1057519824
pharmgkbrs1057519824
gwascentralrs1057519824
openSNPrs1057519824
23andMers1057519824
23andMe allrs1057519824
SNPshotrs1057519824
SNPdbers1057519824
MSV3drs1057519824
GWAS Ctlgrs1057519824
Max Magnitude0
ClinVar
Risk rs1057519824(G;G)
Alt rs1057519824(G;G)
Reference Rs1057519824(T;T)
Significance Probable-Pathogenic
Disease Neoplasm Carcinoma
Variation info
Gene MET
CLNDBN Neoplasm Carcinoma
Reversed 0
HGVS NC_000007.13:g.116423428T>G
CLNSRC
CLNACC RCV000437665.1, RCV000443188.1,