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rs267608111

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs267608111(A;C)
Make rs267608111(C;C)
ReferenceGRCh38 38.1/141
Chromosome2
Position47806202
GeneMSH6
is asnp
is mentioned by
dbSNPrs267608111
ebirs267608111
HLIrs267608111
Exacrs267608111
Varsomers267608111
Maprs267608111
PheGenIrs267608111
hapmaprs267608111
1000 genomesrs267608111
hgdprs267608111
ensemblrs267608111
gopubmedrs267608111
geneviewrs267608111
scholarrs267608111
googlers267608111
pharmgkbrs267608111
gwascentralrs267608111
openSNPrs267608111
23andMers267608111
23andMe allrs267608111
SNP Nexus

SNPshotrs267608111
SNPdbers267608111
MSV3drs267608111
GWAS Ctlgrs267608111
Max Magnitude0
ClinVar
Risk rs267608111(C;C)
Alt rs267608111(C;C)
Reference rs267608111(A;A)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MSH6
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000002.11:g.48033341A>C
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000074903.2,