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rs267608093

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs267608093(-;-)
Make rs267608093(-;T)
ReferenceGRCh38 38.1/141
Chromosome2
Position47803559
GeneMSH6
is asnp
is mentioned by
dbSNPrs267608093
ebirs267608093
HLIrs267608093
Exacrs267608093
Varsomers267608093
Maprs267608093
PheGenIrs267608093
hapmaprs267608093
1000 genomesrs267608093
hgdprs267608093
ensemblrs267608093
gopubmedrs267608093
geneviewrs267608093
scholarrs267608093
googlers267608093
pharmgkbrs267608093
gwascentralrs267608093
openSNPrs267608093
23andMers267608093
23andMe allrs267608093
SNP Nexus

SNPshotrs267608093
SNPdbers267608093
MSV3drs267608093
GWAS Ctlgrs267608093
Max Magnitude0
ClinVar
Risk rs267608093(;)
Alt rs267608093(;)
Reference rs267608093(T;T)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MSH6
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000002.11:g.48030698delT
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000074838.2,