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rs267608118

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs267608118(-;-)
Make rs267608118(-;A)
Make rs267608118(A;A)
ReferenceGRCh38 38.1/141
Chromosome2
Position47806454
GeneFBXO11, MSH6
is asnp
is mentioned by
dbSNPrs267608118
ebirs267608118
HLIrs267608118
Exacrs267608118
Varsomers267608118
Maprs267608118
PheGenIrs267608118
hapmaprs267608118
1000 genomesrs267608118
hgdprs267608118
ensemblrs267608118
gopubmedrs267608118
geneviewrs267608118
scholarrs267608118
googlers267608118
pharmgkbrs267608118
gwascentralrs267608118
openSNPrs267608118
23andMers267608118
23andMe allrs267608118
SNP Nexus

SNPshotrs267608118
SNPdbers267608118
MSV3drs267608118
GWAS Ctlgrs267608118
Max Magnitude0
ClinVar
Risk rs267608118(A;A)
Alt rs267608118(A;A)
Reference rs267608118(;)
Significance Pathogenic
Disease Lynch syndrome Tumor susceptibility linked to germline BAP1 mutations not provided
Variation info
Gene FBXO11 MSH6
CLNDBN Lynch syndrome Tumor susceptibility linked to germline BAP1 mutations not provided
Reversed 0
HGVS NC_000002.11:g.48033593dupA
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000074937.2, RCV000214022.1, RCV000214836.1,