Have questions? Visit https://www.reddit.com/r/SNPedia

rs121434524

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in complete genomics
Make rs121434524(A;A)
Make rs121434524(A;G)
ReferenceGRCh38 38.1/141
Chromosome13
Position26215151
GeneRNF6
is asnp
is mentioned by
dbSNPrs121434524
ebirs121434524
HLIrs121434524
Exacrs121434524
Varsomers121434524
Maprs121434524
PheGenIrs121434524
hapmaprs121434524
1000 genomesrs121434524
hgdprs121434524
ensemblrs121434524
gopubmedrs121434524
geneviewrs121434524
scholarrs121434524
googlers121434524
pharmgkbrs121434524
gwascentralrs121434524
openSNPrs121434524
23andMers121434524
23andMe allrs121434524
SNP Nexus

SNPshotrs121434524
SNPdbers121434524
MSV3drs121434524
GWAS Ctlgrs121434524
Max Magnitude0
OMIM604242
Desc
Variant0003
Relatedalso
ClinVar
Risk rs121434524(A;A)
Alt rs121434524(A;A)
Reference rs121434524(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.26789288C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000006056.4,