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rs267608124

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs267608124(-;-)
Make rs267608124(-;ATCA)
Make rs267608124(ATCA;ATCA)
ReferenceGRCh38 38.1/141
Chromosome2
Position47806634
GeneFBXO11, MSH6
is asnp
is mentioned by
dbSNPrs267608124
ebirs267608124
HLIrs267608124
Exacrs267608124
Varsomers267608124
Maprs267608124
PheGenIrs267608124
hapmaprs267608124
1000 genomesrs267608124
hgdprs267608124
ensemblrs267608124
gopubmedrs267608124
geneviewrs267608124
scholarrs267608124
googlers267608124
pharmgkbrs267608124
gwascentralrs267608124
openSNPrs267608124
23andMers267608124
23andMe allrs267608124
SNP Nexus

SNPshotrs267608124
SNPdbers267608124
MSV3drs267608124
GWAS Ctlgrs267608124
Max Magnitude0
ClinVar
Risk rs267608124(ATCA;ATCA)
Alt rs267608124(ATCA;ATCA)
Reference rs267608124(;)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene FBXO11 MSH6
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000002.11:g.48033773_48033774insATCA
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000074963.2,