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rs121434522

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in complete genomics
Make rs121434522(A;A)
Make rs121434522(A;G)
ReferenceGRCh38 38.1/141
Chromosome13
Position26215577
GeneRNF6
is asnp
is mentioned by
dbSNPrs121434522
ebirs121434522
HLIrs121434522
Exacrs121434522
Varsomers121434522
Maprs121434522
PheGenIrs121434522
hapmaprs121434522
1000 genomesrs121434522
hgdprs121434522
ensemblrs121434522
gopubmedrs121434522
geneviewrs121434522
scholarrs121434522
googlers121434522
pharmgkbrs121434522
gwascentralrs121434522
openSNPrs121434522
23andMers121434522
23andMe allrs121434522
SNP Nexus

SNPshotrs121434522
SNPdbers121434522
MSV3drs121434522
GWAS Ctlgrs121434522
Max Magnitude0
OMIM604242
Desc
Variant0001
Relatedalso
ClinVar
Risk rs121434522(A;A)
Alt rs121434522(A;A)
Reference rs121434522(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.26789714C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000006054.4,