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rs267607955

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(AAGT;AAGT) 0 common in clinvar
Make rs267607955(-;-)
Make rs267607955(-;AAGT)
ReferenceGRCh38 38.1/141
Chromosome2
Position47445616
GeneMSH2
is asnp
is mentioned by
dbSNPrs267607955
ebirs267607955
HLIrs267607955
Exacrs267607955
Varsomers267607955
Maprs267607955
PheGenIrs267607955
hapmaprs267607955
1000 genomesrs267607955
hgdprs267607955
ensemblrs267607955
gopubmedrs267607955
geneviewrs267607955
scholarrs267607955
googlers267607955
pharmgkbrs267607955
gwascentralrs267607955
openSNPrs267607955
23andMers267607955
23andMe allrs267607955
SNP Nexus

SNPshotrs267607955
SNPdbers267607955
MSV3drs267607955
GWAS Ctlgrs267607955
Max Magnitude0
ClinVar
Risk rs267607955(;)
Alt rs267607955(;)
Reference rs267607955(AAGT;AAGT)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MSH2
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000002.11:g.47672755_47672758delAAGT
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000076129.2,