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rs267608058

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(CAGT;CAGT) 0 common in clinvar
(TCAG;TCAG) 0 common in clinvar
Make rs267608058(-;-)
Make rs267608058(-;TCAG)
ReferenceGRCh38 38.1/141
Chromosome2
Position47800133
GeneMSH6
is asnp
is mentioned by
dbSNPrs267608058
ebirs267608058
HLIrs267608058
Exacrs267608058
Varsomers267608058
Maprs267608058
PheGenIrs267608058
hapmaprs267608058
1000 genomesrs267608058
hgdprs267608058
ensemblrs267608058
gopubmedrs267608058
geneviewrs267608058
scholarrs267608058
googlers267608058
pharmgkbrs267608058
gwascentralrs267608058
openSNPrs267608058
23andMers267608058
23andMe allrs267608058
SNP Nexus

SNPshotrs267608058
SNPdbers267608058
MSV3drs267608058
GWAS Ctlgrs267608058
Max Magnitude0
ClinVar
Risk rs267608058(;)
Alt rs267608058(;)
Reference rs267608058(CAGT;CAGT)
Significance Pathogenic
Disease Lynch syndrome Hereditary cancer-predisposing syndrome not provided
Variation info
Gene MSH6
CLNDBN Lynch syndrome Hereditary cancer-predisposing syndrome not provided
Reversed 0
HGVS NC_000002.11:g.48027272_48027275delTCAG
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000074720.2, RCV000162408.2, RCV000202111.2,