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rs267607961

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(AAGAG;AAGAG) 0 common in clinvar
(GAGAA;GAGAA) 0 common in clinvar
Make rs267607961(-;-)
Make rs267607961(-;GAGAA)
ReferenceGRCh38 38.1/141
Chromosome2
Position47463089
GeneMSH2
is asnp
is mentioned by
dbSNPrs267607961
ebirs267607961
HLIrs267607961
Exacrs267607961
Varsomers267607961
Maprs267607961
PheGenIrs267607961
hapmaprs267607961
1000 genomesrs267607961
hgdprs267607961
ensemblrs267607961
gopubmedrs267607961
geneviewrs267607961
scholarrs267607961
googlers267607961
pharmgkbrs267607961
gwascentralrs267607961
openSNPrs267607961
23andMers267607961
23andMe allrs267607961
SNP Nexus

SNPshotrs267607961
SNPdbers267607961
MSV3drs267607961
GWAS Ctlgrs267607961
Max Magnitude0
ClinVar
Risk rs267607961(;)
Alt rs267607961(;)
Reference rs267607961(AAGAG;AAGAG)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MSH2
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000002.11:g.47690228_47690232delGAGAA
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000076163.2,