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rs267608065

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(-;GT) 6 Lynch syndrome, pathogenic mutation
(GT;GT) 0 common in clinvar
(TG;TG) 0 common in clinvar


Make rs267608065(-;-)
ReferenceGRCh38 38.1/141
Chromosome2
Position47800331
GeneMSH6
is asnp
is mentioned by
dbSNPrs267608065
dbSNP (old)rs267608065
ClinGenrs267608065
ebirs267608065
HLIrs267608065
Exacrs267608065
Gnomadrs267608065
Varsomers267608065
Maprs267608065
PheGenIrs267608065
Biobankrs267608065
1000 genomesrs267608065
hgdprs267608065
ensemblrs267608065
gopubmedrs267608065
geneviewrs267608065
scholarrs267608065
googlers267608065
pharmgkbrs267608065
gwascentralrs267608065
openSNPrs267608065
23andMers267608065
23andMe allrs267608065
SNPshotrs267608065
SNPdbers267608065
MSV3drs267608065
GWAS Ctlgrs267608065
Max Magnitude6
ClinVar
Risk rs267608065(-;-)
Alt rs267608065(-;-)
Reference Rs267608065(TG;TG)
Significance Pathogenic
Disease Lynch syndrome Hereditary cancer-predisposing syndrome
Variation info
Gene MSH6
CLNDBN Lynch syndrome Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000002.11:g.48027470_48027471delGT
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000074739.2, RCV000491787.1,