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rs267607970

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs267607970(A;A)
Make rs267607970(A;G)
ReferenceGRCh38 38.1/141
Chromosome2
Position47470964
GeneMSH2
is asnp
is mentioned by
dbSNPrs267607970
ebirs267607970
HLIrs267607970
Exacrs267607970
Varsomers267607970
Maprs267607970
PheGenIrs267607970
hapmaprs267607970
1000 genomesrs267607970
hgdprs267607970
ensemblrs267607970
gopubmedrs267607970
geneviewrs267607970
scholarrs267607970
googlers267607970
pharmgkbrs267607970
gwascentralrs267607970
openSNPrs267607970
23andMers267607970
23andMe allrs267607970
SNP Nexus

SNPshotrs267607970
SNPdbers267607970
MSV3drs267607970
GWAS Ctlgrs267607970
Max Magnitude0
ClinVar
Risk rs267607970(A;A)
Alt rs267607970(A;A)
Reference rs267607970(G;G)
Significance Pathogenic
Disease Turcot syndrome Lynch syndrome
Variation info
Gene MSH2
CLNDBN Turcot syndrome Lynch syndrome
Reversed 0
HGVS NC_000002.11:g.47698103G>A
CLNSRC International Society for Gastrointestinal Hereditary Tumours OMIM Allelic Variant
CLNACC RCV000001836.2, RCV000076224.2,