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rs267608128

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs267608128(-;-)
Make rs267608128(-;ATTA)
Make rs267608128(ATTA;ATTA)
ReferenceGRCh38 38.1/141
Chromosome2
Position47806500
GeneFBXO11, MSH6
is asnp
is mentioned by
dbSNPrs267608128
ebirs267608128
HLIrs267608128
Exacrs267608128
Varsomers267608128
Maprs267608128
PheGenIrs267608128
hapmaprs267608128
1000 genomesrs267608128
hgdprs267608128
ensemblrs267608128
gopubmedrs267608128
geneviewrs267608128
scholarrs267608128
googlers267608128
pharmgkbrs267608128
gwascentralrs267608128
openSNPrs267608128
23andMers267608128
23andMe allrs267608128
SNP Nexus

SNPshotrs267608128
SNPdbers267608128
MSV3drs267608128
GWAS Ctlgrs267608128
Max Magnitude0
ClinVar
Risk rs267608128(ATTA;ATTA)
Alt rs267608128(ATTA;ATTA)
Reference rs267608128(;)
Significance Pathogenic
Disease Lynch syndrome Tumor susceptibility linked to germline BAP1 mutations
Variation info
Gene FBXO11 MSH6
CLNDBN Lynch syndrome Tumor susceptibility linked to germline BAP1 mutations
Reversed 0
HGVS NC_000002.11:g.48033636_48033639dupATTA
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000074943.2, RCV000214756.1,