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rs1057520030

From SNPedia
Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs1057520030(A;T)
Make rs1057520030(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome7
Position116777427
GeneMET
is asnp
is mentioned by
dbSNPrs1057520030
dbSNP (old)rs1057520030
ClinGenrs1057520030
ebirs1057520030
HLIrs1057520030
Exacrs1057520030
Gnomadrs1057520030
Varsomers1057520030
Maprs1057520030
PheGenIrs1057520030
Biobankrs1057520030
1000 genomesrs1057520030
hgdprs1057520030
ensemblrs1057520030
gopubmedrs1057520030
geneviewrs1057520030
scholarrs1057520030
googlers1057520030
pharmgkbrs1057520030
gwascentralrs1057520030
openSNPrs1057520030
23andMers1057520030
23andMe allrs1057520030
SNPshotrs1057520030
SNPdbers1057520030
MSV3drs1057520030
GWAS Ctlgrs1057520030
Max Magnitude0
ClinVar
Risk rs1057520030(T;T)
Alt rs1057520030(T;T)
Reference Rs1057520030(A;A)
Significance Probable-Pathogenic
Disease Carcinoma
Variation info
Gene MET
CLNDBN Carcinoma
Reversed 0
HGVS NC_000007.13:g.116417481A>T
CLNSRC
CLNACC RCV000418101.1,