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rs267607977

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs267607977(-;-)
Make rs267607977(-;A)
Make rs267607977(A;A)
ReferenceGRCh38 38.1/141
Chromosome2
Position47475036
GeneMSH2
is asnp
is mentioned by
dbSNPrs267607977
ebirs267607977
HLIrs267607977
Exacrs267607977
Varsomers267607977
Maprs267607977
PheGenIrs267607977
hapmaprs267607977
1000 genomesrs267607977
hgdprs267607977
ensemblrs267607977
gopubmedrs267607977
geneviewrs267607977
scholarrs267607977
googlers267607977
pharmgkbrs267607977
gwascentralrs267607977
openSNPrs267607977
23andMers267607977
23andMe allrs267607977
SNP Nexus

SNPshotrs267607977
SNPdbers267607977
MSV3drs267607977
GWAS Ctlgrs267607977
Max Magnitude0
ClinVar
Risk rs267607977(A;A)
Alt rs267607977(A;A)
Reference rs267607977(;)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MSH2
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000002.11:g.47702175_47702176insA
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000076280.2,