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rs41341748

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs41341748(A;A)
Make rs41341748(A;G)
ReferenceGRCh38 38.1/141
Chromosome8
Position16155085
GeneMSR1
is asnp
is mentioned by
dbSNPrs41341748
ebirs41341748
HLIrs41341748
Exacrs41341748
Varsomers41341748
Maprs41341748
PheGenIrs41341748
hapmaprs41341748
1000 genomesrs41341748
hgdprs41341748
ensemblrs41341748
gopubmedrs41341748
geneviewrs41341748
scholarrs41341748
googlers41341748
pharmgkbrs41341748
gwascentralrs41341748
openSNPrs41341748
23andMers41341748
23andMe allrs41341748
SNP Nexus

SNPshotrs41341748
SNPdbers41341748
MSV3drs41341748
GWAS Ctlgrs41341748
GMAF0.007805
Max Magnitude0
OMIM153622
Desc
Variant0001
Relatedalso


ClinVar
Risk rs41341748(A,C;A,C)
Alt rs41341748(A,C;A,C)
Reference rs41341748(G;G)
Significance Pathogenic
Disease Malignant tumor of prostate Barrett esophagus/esophageal adenocarcinoma Hereditary cancer-predisposing syndrome
Variation info
Gene MSR1
CLNDBN Malignant tumor of prostate Barrett esophagus/esophageal adenocarcinoma Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000008.10:g.16012594G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000015431.21, RCV000022645.21, RCV000210798.1,