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rs267608121

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs267608121(-;-)
Make rs267608121(-;GTCA)
Make rs267608121(GTCA;GTCA)
ReferenceGRCh38 38.1/141
Chromosome2
Position47806637
GeneFBXO11, MSH6
is asnp
is mentioned by
dbSNPrs267608121
ebirs267608121
HLIrs267608121
Exacrs267608121
Varsomers267608121
Maprs267608121
PheGenIrs267608121
hapmaprs267608121
1000 genomesrs267608121
hgdprs267608121
ensemblrs267608121
gopubmedrs267608121
geneviewrs267608121
scholarrs267608121
googlers267608121
pharmgkbrs267608121
gwascentralrs267608121
openSNPrs267608121
23andMers267608121
23andMe allrs267608121
SNP Nexus

SNPshotrs267608121
SNPdbers267608121
MSV3drs267608121
GWAS Ctlgrs267608121
Max Magnitude0
ClinVar
Risk rs267608121(TCAG;TCAG)
Alt rs267608121(TCAG;TCAG)
Reference rs267608121(;)
Significance Pathogenic
Disease Lynch syndrome Hereditary cancer-predisposing syndrome not provided
Variation info
Gene FBXO11 MSH6
CLNDBN Lynch syndrome Hereditary cancer-predisposing syndrome not provided
Reversed 0
HGVS NC_000002.11:g.48033773_48033776dupGTCA
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000074964.3, RCV000131963.4, RCV000202165.1,