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rs267607931

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(ATGA;ATGA) 0 common in clinvar
(GAAT;GAAT) 0 common in clinvar
Make rs267607931(-;-)
Make rs267607931(-;GAAT)
ReferenceGRCh38 38.1/141
Chromosome2
Position47412527
GeneMSH2
is asnp
is mentioned by
dbSNPrs267607931
ebirs267607931
HLIrs267607931
Exacrs267607931
Varsomers267607931
Maprs267607931
PheGenIrs267607931
hapmaprs267607931
1000 genomesrs267607931
hgdprs267607931
ensemblrs267607931
gopubmedrs267607931
geneviewrs267607931
scholarrs267607931
googlers267607931
pharmgkbrs267607931
gwascentralrs267607931
openSNPrs267607931
23andMers267607931
23andMe allrs267607931
SNP Nexus

SNPshotrs267607931
SNPdbers267607931
MSV3drs267607931
GWAS Ctlgrs267607931
Max Magnitude0
ClinVar
Risk rs267607931(;)
Alt rs267607931(;)
Reference rs267607931(ATGA;ATGA)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MSH2
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000002.11:g.47639666_47639669delGAAT
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000076701.2,