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rs267608126

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs267608126(-;-)
Make rs267608126(-;TTCA)
Make rs267608126(TTCA;TTCA)
ReferenceGRCh38 38.1/141
Chromosome2
Position47806591
GeneFBXO11, MSH6
is asnp
is mentioned by
dbSNPrs267608126
ebirs267608126
HLIrs267608126
Exacrs267608126
Varsomers267608126
Maprs267608126
PheGenIrs267608126
hapmaprs267608126
1000 genomesrs267608126
hgdprs267608126
ensemblrs267608126
gopubmedrs267608126
geneviewrs267608126
scholarrs267608126
googlers267608126
pharmgkbrs267608126
gwascentralrs267608126
openSNPrs267608126
23andMers267608126
23andMe allrs267608126
SNP Nexus

SNPshotrs267608126
SNPdbers267608126
MSV3drs267608126
GWAS Ctlgrs267608126
Max Magnitude0
ClinVar
Risk rs267608126(ATTC;ATTC)
Alt rs267608126(ATTC;ATTC)
Reference rs267608126(;)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene FBXO11 MSH6
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000002.11:g.48033727_48033730dupTTCA
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000074953.2,