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rs267607949

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs267607949(A;G)
Make rs267607949(G;G)
ReferenceGRCh38 38.1/141
Chromosome2
Position47445546
GeneMSH2
is asnp
is mentioned by
dbSNPrs267607949
ebirs267607949
HLIrs267607949
Exacrs267607949
Varsomers267607949
Maprs267607949
PheGenIrs267607949
hapmaprs267607949
1000 genomesrs267607949
hgdprs267607949
ensemblrs267607949
gopubmedrs267607949
geneviewrs267607949
scholarrs267607949
googlers267607949
pharmgkbrs267607949
gwascentralrs267607949
openSNPrs267607949
23andMers267607949
23andMe allrs267607949
SNP Nexus

SNPshotrs267607949
SNPdbers267607949
MSV3drs267607949
GWAS Ctlgrs267607949
Max Magnitude0
ClinVar
Risk rs267607949(C,G;C,G)
Alt rs267607949(C,G;C,G)
Reference rs267607949(A;A)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MSH2
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000002.11:g.47672685A>C; NC_000002.11:g.47672685A>G
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000076100.2, RCV000076101.2,