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rs387906645

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs387906645(C;G)
Make rs387906645(G;G)
ReferenceGRCh38 38.1/141
Chromosome8
Position16164122
GeneMSR1
is asnp
is mentioned by
dbSNPrs387906645
ebirs387906645
HLIrs387906645
Exacrs387906645
Varsomers387906645
Maprs387906645
PheGenIrs387906645
hapmaprs387906645
1000 genomesrs387906645
hgdprs387906645
ensemblrs387906645
gopubmedrs387906645
geneviewrs387906645
scholarrs387906645
googlers387906645
pharmgkbrs387906645
gwascentralrs387906645
openSNPrs387906645
23andMers387906645
23andMe allrs387906645
SNP Nexus

SNPshotrs387906645
SNPdbers387906645
MSV3drs387906645
GWAS Ctlgrs387906645
Max Magnitude0
ClinVar
Risk rs387906645(G;G)
Alt rs387906645(G;G)
Reference rs387906645(C;C)
Significance Pathogenic
Disease Barrett esophagus/esophageal adenocarcinoma
Variation info
Gene MSR1
CLNDBN Barrett esophagus/esophageal adenocarcinoma
Reversed 1
HGVS NC_000008.10:g.16021631G>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000022646.26,