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rs387907029

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs387907029(A;C)
Make rs387907029(C;C)
ReferenceGRCh38 38.1/141
Chromosome8
Position103371787
GeneCTHRC1
is asnp
is mentioned by
dbSNPrs387907029
ebirs387907029
HLIrs387907029
Exacrs387907029
Varsomers387907029
Maprs387907029
PheGenIrs387907029
hapmaprs387907029
1000 genomesrs387907029
hgdprs387907029
ensemblrs387907029
gopubmedrs387907029
geneviewrs387907029
scholarrs387907029
googlers387907029
pharmgkbrs387907029
gwascentralrs387907029
openSNPrs387907029
23andMers387907029
23andMe allrs387907029
SNP Nexus

SNPshotrs387907029
SNPdbers387907029
MSV3drs387907029
GWAS Ctlgrs387907029
Max Magnitude0
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
CLNACC RCV000023833.2,