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rs267608127

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs267608127(-;-)
Make rs267608127(-;AAGT)
Make rs267608127(AAGT;AAGT)
ReferenceGRCh38 38.1/141
Chromosome2
Position47806585
GeneFBXO11, MSH6
is asnp
is mentioned by
dbSNPrs267608127
ebirs267608127
HLIrs267608127
Exacrs267608127
Varsomers267608127
Maprs267608127
PheGenIrs267608127
hapmaprs267608127
1000 genomesrs267608127
hgdprs267608127
ensemblrs267608127
gopubmedrs267608127
geneviewrs267608127
scholarrs267608127
googlers267608127
pharmgkbrs267608127
gwascentralrs267608127
openSNPrs267608127
23andMers267608127
23andMe allrs267608127
SNP Nexus

SNPshotrs267608127
SNPdbers267608127
MSV3drs267608127
GWAS Ctlgrs267608127
Max Magnitude0
ClinVar
Risk rs267608127(AAGT;AAGT)
Alt rs267608127(AAGT;AAGT)
Reference rs267608127(;)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene FBXO11 MSH6
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000002.11:g.48033721_48033724dupAAGT
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000074951.2,