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rs267608009

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs267608009(-;-)
Make rs267608009(-;C)
ReferenceGRCh38 38.1/141
Chromosome2
Position47478322
GeneMSH2
is asnp
is mentioned by
dbSNPrs267608009
ebirs267608009
HLIrs267608009
Exacrs267608009
Varsomers267608009
Maprs267608009
PheGenIrs267608009
hapmaprs267608009
1000 genomesrs267608009
hgdprs267608009
ensemblrs267608009
gopubmedrs267608009
geneviewrs267608009
scholarrs267608009
googlers267608009
pharmgkbrs267608009
gwascentralrs267608009
openSNPrs267608009
23andMers267608009
23andMe allrs267608009
SNP Nexus

SNPshotrs267608009
SNPdbers267608009
MSV3drs267608009
GWAS Ctlgrs267608009
Max Magnitude0
ClinVar
Risk rs267608009(;)
Alt rs267608009(;)
Reference rs267608009(C;C)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MSH2
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000002.11:g.47705461delC
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000076446.2,