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rs267607928

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs267607928(-;-)
Make rs267607928(-;T)
ReferenceGRCh38 38.1/141
Chromosome2
Position47410278
GeneMSH2
is asnp
is mentioned by
dbSNPrs267607928
ebirs267607928
HLIrs267607928
Exacrs267607928
Varsomers267607928
Maprs267607928
PheGenIrs267607928
hapmaprs267607928
1000 genomesrs267607928
hgdprs267607928
ensemblrs267607928
gopubmedrs267607928
geneviewrs267607928
scholarrs267607928
googlers267607928
pharmgkbrs267607928
gwascentralrs267607928
openSNPrs267607928
23andMers267607928
23andMe allrs267607928
SNP Nexus

SNPshotrs267607928
SNPdbers267607928
MSV3drs267607928
GWAS Ctlgrs267607928
Max Magnitude0
ClinVar
Risk rs267607928(;)
Alt rs267607928(;)
Reference rs267607928(T;T)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MSH2
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000002.11:g.47637417delT
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000076636.2,