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rs267607983

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs267607983(A;A)
Make rs267607983(A;C)
ReferenceGRCh38 38.1/141
Chromosome2
Position47475220
GeneMSH2
is asnp
is mentioned by
dbSNPrs267607983
ebirs267607983
HLIrs267607983
Exacrs267607983
Varsomers267607983
Maprs267607983
PheGenIrs267607983
hapmaprs267607983
1000 genomesrs267607983
hgdprs267607983
ensemblrs267607983
gopubmedrs267607983
geneviewrs267607983
scholarrs267607983
googlers267607983
pharmgkbrs267607983
gwascentralrs267607983
openSNPrs267607983
23andMers267607983
23andMe allrs267607983
SNP Nexus

SNPshotrs267607983
SNPdbers267607983
MSV3drs267607983
GWAS Ctlgrs267607983
Max Magnitude0
ClinVar
Risk rs267607983(A;A)
Alt rs267607983(A;A)
Reference rs267607983(C;C)
Significance Probable-Pathogenic
Disease Lynch syndrome
Variation info
Gene MSH2
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000002.11:g.47702359C>A
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000076325.2,