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rs267608086

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs267608086(G;T)
Make rs267608086(T;T)
ReferenceGRCh38 38.1/141
Chromosome2
Position47803614
GeneMSH6
is asnp
is mentioned by
dbSNPrs267608086
ebirs267608086
HLIrs267608086
Exacrs267608086
Varsomers267608086
Maprs267608086
PheGenIrs267608086
hapmaprs267608086
1000 genomesrs267608086
hgdprs267608086
ensemblrs267608086
gopubmedrs267608086
geneviewrs267608086
scholarrs267608086
googlers267608086
pharmgkbrs267608086
gwascentralrs267608086
openSNPrs267608086
23andMers267608086
23andMe allrs267608086
SNP Nexus

SNPshotrs267608086
SNPdbers267608086
MSV3drs267608086
GWAS Ctlgrs267608086
Max Magnitude0
ClinVar
Risk rs267608086(T;T)
Alt rs267608086(T;T)
Reference rs267608086(G;G)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MSH6
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000002.11:g.48030753G>T
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000074843.2,