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rs267608068

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs267608068(A;A)
Make rs267608068(A;T)
ReferenceGRCh38 38.1/141
Chromosome2
Position47800044
GeneMSH6
is asnp
is mentioned by
dbSNPrs267608068
ebirs267608068
HLIrs267608068
Exacrs267608068
Varsomers267608068
Maprs267608068
PheGenIrs267608068
hapmaprs267608068
1000 genomesrs267608068
hgdprs267608068
ensemblrs267608068
gopubmedrs267608068
geneviewrs267608068
scholarrs267608068
googlers267608068
pharmgkbrs267608068
gwascentralrs267608068
openSNPrs267608068
23andMers267608068
23andMe allrs267608068
SNP Nexus

SNPshotrs267608068
SNPdbers267608068
MSV3drs267608068
GWAS Ctlgrs267608068
Max Magnitude0
ClinVar
Risk rs267608068(A;A)
Alt rs267608068(A;A)
Reference rs267608068(T;T)
Significance Pathogenic
Disease Lynch syndrome Hereditary cancer-predisposing syndrome not provided
Variation info
Gene MSH6
CLNDBN Lynch syndrome Hereditary cancer-predisposing syndrome not provided
Reversed 0
HGVS NC_000002.11:g.48027183T>A
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000074710.2, RCV000162397.1, RCV000201965.1,