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rs267608056

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs267608056(-;-)
Make rs267608056(-;C)
ReferenceGRCh38 38.1/141
Chromosome2
Position47799068
GeneMSH6
is asnp
is mentioned by
dbSNPrs267608056
ebirs267608056
HLIrs267608056
Exacrs267608056
Varsomers267608056
Maprs267608056
PheGenIrs267608056
hapmaprs267608056
1000 genomesrs267608056
hgdprs267608056
ensemblrs267608056
gopubmedrs267608056
geneviewrs267608056
scholarrs267608056
googlers267608056
pharmgkbrs267608056
gwascentralrs267608056
openSNPrs267608056
23andMers267608056
23andMe allrs267608056
SNP Nexus

SNPshotrs267608056
SNPdbers267608056
MSV3drs267608056
GWAS Ctlgrs267608056
Max Magnitude0
ClinVar
Risk rs267608056(;)
Alt rs267608056(;)
Reference rs267608056(C;C)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MSH6
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000002.11:g.48026207delC
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000074630.2,