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rs267607940

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs267607940(G;T)
Make rs267607940(T;T)
ReferenceGRCh38 38.1/141
Chromosome2
Position47416430
GeneMSH2
is asnp
is mentioned by
dbSNPrs267607940
ebirs267607940
HLIrs267607940
Exacrs267607940
Varsomers267607940
Maprs267607940
PheGenIrs267607940
hapmaprs267607940
1000 genomesrs267607940
hgdprs267607940
ensemblrs267607940
gopubmedrs267607940
geneviewrs267607940
scholarrs267607940
googlers267607940
pharmgkbrs267607940
gwascentralrs267607940
openSNPrs267607940
23andMers267607940
23andMe allrs267607940
SNP Nexus

SNPshotrs267607940
SNPdbers267607940
MSV3drs267607940
GWAS Ctlgrs267607940
Max Magnitude0
ClinVar
Risk rs267607940(A,T;A,T)
Alt rs267607940(A,T;A,T)
Reference rs267607940(G;G)
Significance Pathogenic
Disease Lynch syndrome Hereditary cancer-predisposing syndrome
Variation info
Gene MSH2
CLNDBN Lynch syndrome Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000002.11:g.47643569G>A; NC_000002.11:g.47643569G>T
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000076014.2, RCV000132414.2, RCV000076015.2,