rs121912967

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(T;T)	0	common in clinvar

Make rs121912967(C;C)

Make rs121912967(C;T)

Reference

GRCh38 38.1/141

Chromosome

18

Position

52906134

Gene

DCC

is a	snp
is	mentioned by
dbSNP	rs121912967
dbSNP (classic)	rs121912967
ClinGen	rs121912967
ebi	rs121912967
HLI	rs121912967
Exac	rs121912967
Gnomad	rs121912967
Varsome	rs121912967
LitVar	rs121912967
Map	rs121912967
PheGenI	rs121912967
Biobank	rs121912967
1000 genomes	rs121912967
hgdp	rs121912967
ensembl	rs121912967
geneview	rs121912967
scholar	rs121912967
google	rs121912967
pharmgkb	rs121912967
gwascentral	rs121912967
openSNP	rs121912967
23andMe	rs121912967
SNPshot	rs121912967
SNPdbe	rs121912967
MSV3d	rs121912967
GWAS Ctlg	rs121912967

Max Magnitude

0

OMIM	120470
Desc
Variant	0002
Related	also

ClinVar
Risk	rs121912967(C;C)
Alt	rs121912967(C;C)
Reference	Rs121912967(T;T)
Significance	Pathogenic
Disease	Esophageal carcinoma
Variation	info
Gene	DCC
CLNDBN	Esophageal carcinoma, somatic
Reversed	0
HGVS	NC_000018.9:g.50432504T>C
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000018604.4,