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rs2303425

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs2303425(C;C)
Make rs2303425(C;T)
ReferenceGRCh38 38.1/141
Chromosome2
Position47403074
GeneMSH2
is asnp
is mentioned by
dbSNPrs2303425
ebirs2303425
HLIrs2303425
Exacrs2303425
Varsomers2303425
Maprs2303425
PheGenIrs2303425
hapmaprs2303425
1000 genomesrs2303425
hgdprs2303425
ensemblrs2303425
gopubmedrs2303425
geneviewrs2303425
scholarrs2303425
googlers2303425
pharmgkbrs2303425
gwascentralrs2303425
openSNPrs2303425
23andMers2303425
23andMe allrs2303425
SNP Nexus

SNPshotrs2303425
SNPdbers2303425
MSV3drs2303425
GWAS Ctlgrs2303425
Max Magnitude0

[PMID 25252909] Mismatch Repair Gene Polymorphisms and Association with Lung Cancer Development

ClinVar
Risk rs2303425(C;C)
Alt rs2303425(C;C)
Reference rs2303425(T;T)
Significance Non-pathogenic
Disease Lynch syndrome Hereditary cancer-predisposing syndrome
Variation info
Gene MSH2
CLNDBN Lynch syndrome Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000002.11:g.47630213T>C
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000075980.2, RCV000162385.1,


[PMID 26975740] MSH2 rs2303425 Polymorphism is Associated with Early-Onset Breast Cancer in Taiwan.