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rs267608042

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(TT;TT) 0 common in clinvar
Make rs267608042(-;-)
Make rs267608042(-;TT)
ReferenceGRCh38 38.1/141
Chromosome2
Position47801102
GeneMSH6
is asnp
is mentioned by
dbSNPrs267608042
ebirs267608042
HLIrs267608042
Exacrs267608042
Varsomers267608042
Maprs267608042
PheGenIrs267608042
hapmaprs267608042
1000 genomesrs267608042
hgdprs267608042
ensemblrs267608042
gopubmedrs267608042
geneviewrs267608042
scholarrs267608042
googlers267608042
pharmgkbrs267608042
gwascentralrs267608042
openSNPrs267608042
23andMers267608042
23andMe allrs267608042
SNP Nexus

SNPshotrs267608042
SNPdbers267608042
MSV3drs267608042
GWAS Ctlgrs267608042
Max Magnitude0
ClinVar
Risk rs267608042(;)
Alt rs267608042(;)
Reference rs267608042(TT;TT)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MSH6
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000002.11:g.48028241_48028242delTT
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000074804.2,