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rs267607984

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs267607984(-;-)
Make rs267607984(-;C)
ReferenceGRCh38 38.1/141
Chromosome2
Position47475118
GeneMSH2
is asnp
is mentioned by
dbSNPrs267607984
ebirs267607984
HLIrs267607984
Exacrs267607984
Varsomers267607984
Maprs267607984
PheGenIrs267607984
hapmaprs267607984
1000 genomesrs267607984
hgdprs267607984
ensemblrs267607984
gopubmedrs267607984
geneviewrs267607984
scholarrs267607984
googlers267607984
pharmgkbrs267607984
gwascentralrs267607984
openSNPrs267607984
23andMers267607984
23andMe allrs267607984
SNP Nexus

SNPshotrs267607984
SNPdbers267607984
MSV3drs267607984
GWAS Ctlgrs267607984
Max Magnitude0
ClinVar
Risk rs267607984(;)
Alt rs267607984(;)
Reference rs267607984(C;C)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MSH2
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000002.11:g.47702257delC
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000076301.2,