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rs267608112

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(TAACAG;TAACAG) 0 common in clinvar
Make rs267608112(-;-)
Make rs267608112(-;TAACAG)
ReferenceGRCh38 38.1/141
Chromosome2
Position47806198
GeneMSH6
is asnp
is mentioned by
dbSNPrs267608112
ebirs267608112
HLIrs267608112
Exacrs267608112
Varsomers267608112
Maprs267608112
PheGenIrs267608112
hapmaprs267608112
1000 genomesrs267608112
hgdprs267608112
ensemblrs267608112
gopubmedrs267608112
geneviewrs267608112
scholarrs267608112
googlers267608112
pharmgkbrs267608112
gwascentralrs267608112
openSNPrs267608112
23andMers267608112
23andMe allrs267608112
SNP Nexus

SNPshotrs267608112
SNPdbers267608112
MSV3drs267608112
GWAS Ctlgrs267608112
Max Magnitude0
ClinVar
Risk rs267608112(;)
Alt rs267608112(;)
Reference rs267608112(TAACAG;TAACAG)
Significance Probable-Pathogenic
Disease Lynch syndrome
Variation info
Gene MSH6
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000002.11:g.48033337_48033342delTAACAG
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000074908.2,