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rs267608050

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs267608050(-;-)
Make rs267608050(-;T)
ReferenceGRCh38 38.1/141
Chromosome2
Position47799767
GeneMSH6
is asnp
is mentioned by
dbSNPrs267608050
dbSNP (old)rs267608050
ClinGenrs267608050
ebirs267608050
HLIrs267608050
Exacrs267608050
Varsomers267608050
Maprs267608050
PheGenIrs267608050
Biobankrs267608050
1000 genomesrs267608050
hgdprs267608050
ensemblrs267608050
gopubmedrs267608050
geneviewrs267608050
scholarrs267608050
googlers267608050
pharmgkbrs267608050
gwascentralrs267608050
openSNPrs267608050
23andMers267608050
23andMe allrs267608050
SNP Nexus

SNPshotrs267608050
SNPdbers267608050
MSV3drs267608050
GWAS Ctlgrs267608050
Max Magnitude0
ClinVar
Risk rs267608050(-;-)
Alt rs267608050(-;-)
Reference Rs267608050(T;T)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MSH6
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000002.11:g.48026906delT
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000074686.2,