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rs119473032

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in complete genomics
Make rs119473032(A;G)
Make rs119473032(G;G)
ReferenceGRCh38 38.1/141
Chromosome8
Position20253576
GeneLZTS1
is asnp
is mentioned by
dbSNPrs119473032
ebirs119473032
HLIrs119473032
Exacrs119473032
Varsomers119473032
Maprs119473032
PheGenIrs119473032
hapmaprs119473032
1000 genomesrs119473032
hgdprs119473032
ensemblrs119473032
gopubmedrs119473032
geneviewrs119473032
scholarrs119473032
googlers119473032
pharmgkbrs119473032
gwascentralrs119473032
openSNPrs119473032
23andMers119473032
23andMe allrs119473032
SNP Nexus

SNPshotrs119473032
SNPdbers119473032
MSV3drs119473032
GWAS Ctlgrs119473032
Max Magnitude0
OMIM606551
Desc
Variant0002
Relatedalso
ClinVar
Risk rs119473032(G;G)
Alt rs119473032(G;G)
Reference rs119473032(A;A)
Significance Pathogenic
Disease Esophageal squamous cell carcinoma
Variation info
Gene LZTS1
CLNDBN Esophageal squamous cell carcinoma, somatic
Reversed 1
HGVS NC_000008.10:g.20111087T>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000004468.4,