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rs267608082

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(TG;TG) 0 common in clinvar
Make rs267608082(-;-)
Make rs267608082(-;TG)
ReferenceGRCh38 38.1/141
Chromosome2
Position47799884
GeneMSH6
is asnp
is mentioned by
dbSNPrs267608082
ebirs267608082
HLIrs267608082
Exacrs267608082
Varsomers267608082
Maprs267608082
PheGenIrs267608082
hapmaprs267608082
1000 genomesrs267608082
hgdprs267608082
ensemblrs267608082
gopubmedrs267608082
geneviewrs267608082
scholarrs267608082
googlers267608082
pharmgkbrs267608082
gwascentralrs267608082
openSNPrs267608082
23andMers267608082
23andMe allrs267608082
SNP Nexus

SNPshotrs267608082
SNPdbers267608082
MSV3drs267608082
GWAS Ctlgrs267608082
Max Magnitude0
ClinVar
Risk rs267608082(;)
Alt rs267608082(;)
Reference rs267608082(TG;TG)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MSH6
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000002.11:g.48027023_48027024delTG
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000074696.2,