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rs267608094

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs267608094(C;T)
Make rs267608094(T;T)
ReferenceGRCh38 38.1/141
Chromosome2
Position47806641
GeneFBXO11, MSH6
is asnp
is mentioned by
dbSNPrs267608094
ebirs267608094
HLIrs267608094
Exacrs267608094
Varsomers267608094
Maprs267608094
PheGenIrs267608094
hapmaprs267608094
1000 genomesrs267608094
hgdprs267608094
ensemblrs267608094
gopubmedrs267608094
geneviewrs267608094
scholarrs267608094
googlers267608094
pharmgkbrs267608094
gwascentralrs267608094
openSNPrs267608094
23andMers267608094
23andMe allrs267608094
SNP Nexus

SNPshotrs267608094
SNPdbers267608094
MSV3drs267608094
GWAS Ctlgrs267608094
Max Magnitude0
ClinVar
Risk rs267608094(T;T)
Alt rs267608094(T;T)
Reference rs267608094(C;C)
Significance Other
Disease Lynch syndrome Hereditary cancer-predisposing syndrome not provided
Variation info
Gene FBXO11 MSH6
CLNDBN Lynch syndrome Hereditary cancer-predisposing syndrome not provided
Reversed 0
HGVS NC_000002.11:g.48033780C>T
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000035325.5, RCV000131743.4, RCV000202305.1,