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rs267608091

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs267608091(-;-)
Make rs267608091(-;T)
Make rs267608091(T;T)
ReferenceGRCh38 38.1/141
Chromosome2
Position47803510
GeneMSH6
is asnp
is mentioned by
dbSNPrs267608091
ebirs267608091
HLIrs267608091
Exacrs267608091
Varsomers267608091
Maprs267608091
PheGenIrs267608091
hapmaprs267608091
1000 genomesrs267608091
hgdprs267608091
ensemblrs267608091
gopubmedrs267608091
geneviewrs267608091
scholarrs267608091
googlers267608091
pharmgkbrs267608091
gwascentralrs267608091
openSNPrs267608091
23andMers267608091
23andMe allrs267608091
SNP Nexus

SNPshotrs267608091
SNPdbers267608091
MSV3drs267608091
GWAS Ctlgrs267608091
Max Magnitude0
ClinVar
Risk rs267608091(T;T)
Alt rs267608091(T;T)
Reference rs267608091(;)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MSH6
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000002.11:g.48030649dupT
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000074832.2,