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rs146370051

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs146370051(C;C)
Make rs146370051(C;T)
ReferenceGRCh38 38.1/141
Chromosome10
Position72133059
GeneASCC1
is asnp
is mentioned by
dbSNPrs146370051
ebirs146370051
HLIrs146370051
Exacrs146370051
Varsomers146370051
Maprs146370051
PheGenIrs146370051
hapmaprs146370051
1000 genomesrs146370051
hgdprs146370051
ensemblrs146370051
gopubmedrs146370051
geneviewrs146370051
scholarrs146370051
googlers146370051
pharmgkbrs146370051
gwascentralrs146370051
openSNPrs146370051
23andMers146370051
23andMe allrs146370051
SNP Nexus

SNPshotrs146370051
SNPdbers146370051
MSV3drs146370051
GWAS Ctlgrs146370051
GMAF0.001837
Max Magnitude0
ClinVar
Risk rs146370051(C;C)
Alt rs146370051(C;C)
Reference rs146370051(T;T)
Significance Pathogenic
Disease Barrett esophagus/esophageal adenocarcinoma
Variation info
Gene ASCC1
CLNDBN Barrett esophagus/esophageal adenocarcinoma
Reversed 0
HGVS NC_000010.10:g.73892817T>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000024125.2,