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rs267608090

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs267608090(-;-)
Make rs267608090(-;T)
ReferenceGRCh38 38.1/141
Chromosome2
Position47803468
GeneMSH6
is asnp
is mentioned by
dbSNPrs267608090
ebirs267608090
HLIrs267608090
Exacrs267608090
Varsomers267608090
Maprs267608090
PheGenIrs267608090
hapmaprs267608090
1000 genomesrs267608090
hgdprs267608090
ensemblrs267608090
gopubmedrs267608090
geneviewrs267608090
scholarrs267608090
googlers267608090
pharmgkbrs267608090
gwascentralrs267608090
openSNPrs267608090
23andMers267608090
23andMe allrs267608090
SNP Nexus

SNPshotrs267608090
SNPdbers267608090
MSV3drs267608090
GWAS Ctlgrs267608090
Max Magnitude0
ClinVar
Risk rs267608090(;)
Alt rs267608090(;)
Reference rs267608090(T;T)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MSH6
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000002.11:g.48030607delT
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000074822.2,