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rs267608130

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(AAAGCTA;AAAGCTA) 0 common in clinvar
(CTAAAAG;CTAAAAG) 0 common in clinvar
Make rs267608130(-;-)
Make rs267608130(-;AAAGCTA)
ReferenceGRCh38 38.1/141
Chromosome2
Position47806537
GeneFBXO11, MSH6
is asnp
is mentioned by
dbSNPrs267608130
ebirs267608130
HLIrs267608130
Exacrs267608130
Varsomers267608130
Maprs267608130
PheGenIrs267608130
hapmaprs267608130
1000 genomesrs267608130
hgdprs267608130
ensemblrs267608130
gopubmedrs267608130
geneviewrs267608130
scholarrs267608130
googlers267608130
pharmgkbrs267608130
gwascentralrs267608130
openSNPrs267608130
23andMers267608130
23andMe allrs267608130
SNP Nexus

SNPshotrs267608130
SNPdbers267608130
MSV3drs267608130
GWAS Ctlgrs267608130
Max Magnitude0
ClinVar
Risk rs267608130(;)
Alt rs267608130(;)
Reference rs267608130(CTAAAAG;CTAAAAG)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene FBXO11 MSH6
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000002.11:g.48033676_48033682delAAAGCTA
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000074946.2,