rs121434523

Orientation

minus

Stabilized

minus

Geno	Mag	Summary
(G;G)	0	common in complete genomics

Make rs121434523(A;A)

Make rs121434523(A;G)

Reference

GRCh38 38.1/141

Chromosome

13

Position

26215158

Gene

RNF6

is a	snp
is	mentioned by
dbSNP	rs121434523
dbSNP (classic)	rs121434523
ClinGen	rs121434523
ebi	rs121434523
HLI	rs121434523
Exac	rs121434523
Gnomad	rs121434523
Varsome	rs121434523
LitVar	rs121434523
Map	rs121434523
PheGenI	rs121434523
Biobank	rs121434523
1000 genomes	rs121434523
hgdp	rs121434523
ensembl	rs121434523
geneview	rs121434523
scholar	rs121434523
google	rs121434523
pharmgkb	rs121434523
gwascentral	rs121434523
openSNP	rs121434523
23andMe	rs121434523
SNPshot	rs121434523
SNPdbe	rs121434523
MSV3d	rs121434523
GWAS Ctlg	rs121434523

Max Magnitude

0

OMIM	604242
Desc
Variant	0002
Related	also

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 UniProtKB (protein)
CLNACC	RCV000006055.4,