rs121434522

Orientation

minus

Stabilized

minus

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

Make rs121434522(A;A)

Make rs121434522(A;G)

Reference

GRCh38 38.1/141

Chromosome

13

Position

26215577

Gene

RNF6

is a	snp
is	mentioned by
dbSNP	rs121434522
dbSNP (classic)	rs121434522
ClinGen	rs121434522
ebi	rs121434522
HLI	rs121434522
Exac	rs121434522
Gnomad	rs121434522
Varsome	rs121434522
LitVar	rs121434522
Map	rs121434522
PheGenI	rs121434522
Biobank	rs121434522
1000 genomes	rs121434522
hgdp	rs121434522
ensembl	rs121434522
geneview	rs121434522
scholar	rs121434522
google	rs121434522
pharmgkb	rs121434522
gwascentral	rs121434522
openSNP	rs121434522
23andMe	rs121434522
SNPshot	rs121434522
SNPdbe	rs121434522
MSV3d	rs121434522
GWAS Ctlg	rs121434522

Max Magnitude

0

OMIM	604242
Desc
Variant	0001
Related	also

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 UniProtKB (protein)
CLNACC	RCV000006054.4,