rs387907029

Orientation

plus

Stabilized

plus

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

Make rs387907029(A;C)

Make rs387907029(C;C)

Reference

GRCh38 38.1/141

Chromosome

8

Position

103371787

Gene

CTHRC1

is a	snp
is	mentioned by
dbSNP	rs387907029
dbSNP (classic)	rs387907029
ClinGen	rs387907029
ebi	rs387907029
HLI	rs387907029
Exac	rs387907029
Gnomad	rs387907029
Varsome	rs387907029
LitVar	rs387907029
Map	rs387907029
PheGenI	rs387907029
Biobank	rs387907029
1000 genomes	rs387907029
hgdp	rs387907029
ensembl	rs387907029
geneview	rs387907029
scholar	rs387907029
google	rs387907029
pharmgkb	rs387907029
gwascentral	rs387907029
openSNP	rs387907029
23andMe	rs387907029
SNPshot	rs387907029
SNPdbe	rs387907029
MSV3d	rs387907029
GWAS Ctlg	rs387907029

Max Magnitude

0

ClinVar
Risk	rs387907029(C;C)
Alt	rs387907029(C;C)
Reference	Rs387907029(A;A)
Significance	Pathogenic
Disease	Barrett esophagus/esophageal adenocarcinoma
Variation	info
Gene	CTHRC1
CLNDBN	Barrett esophagus/esophageal adenocarcinoma
Reversed	0
HGVS	NC_000008.10:g.104384015A>C
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000023833.2,