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rs121434523

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in complete genomics
Make rs121434523(A;A)
Make rs121434523(A;G)
ReferenceGRCh38 38.1/141
Chromosome13
Position26215158
GeneRNF6
is asnp
is mentioned by
dbSNPrs121434523
ebirs121434523
HLIrs121434523
Exacrs121434523
Varsomers121434523
Maprs121434523
PheGenIrs121434523
hapmaprs121434523
1000 genomesrs121434523
hgdprs121434523
ensemblrs121434523
gopubmedrs121434523
geneviewrs121434523
scholarrs121434523
googlers121434523
pharmgkbrs121434523
gwascentralrs121434523
openSNPrs121434523
23andMers121434523
23andMe allrs121434523
SNP Nexus

SNPshotrs121434523
SNPdbers121434523
MSV3drs121434523
GWAS Ctlgrs121434523
Max Magnitude0
OMIM604242
Desc
Variant0002
Relatedalso
ClinVar
Risk rs121434523(A;A)
Alt rs121434523(A;A)
Reference rs121434523(G;G)
Significance Pathogenic
Disease Esophageal squamous cell carcinoma
Variation info
Gene RNF6
CLNDBN Esophageal squamous cell carcinoma, somatic
Reversed 1
HGVS NC_000013.10:g.26789295C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000006055.4,