Have questions? Visit https://www.reddit.com/r/SNPedia

rs267608096

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs267608096(A;A)
Make rs267608096(A;G)
ReferenceGRCh38 38.1/141
Chromosome2
Position47803686
GeneMSH6
is asnp
is mentioned by
dbSNPrs267608096
ebirs267608096
HLIrs267608096
Exacrs267608096
Varsomers267608096
Maprs267608096
PheGenIrs267608096
hapmaprs267608096
1000 genomesrs267608096
hgdprs267608096
ensemblrs267608096
gopubmedrs267608096
geneviewrs267608096
scholarrs267608096
googlers267608096
pharmgkbrs267608096
gwascentralrs267608096
openSNPrs267608096
23andMers267608096
23andMe allrs267608096
SNP Nexus

SNPshotrs267608096
SNPdbers267608096
MSV3drs267608096
GWAS Ctlgrs267608096
Max Magnitude0
ClinVar
Risk rs267608096(A;A)
Alt rs267608096(A;A)
Reference rs267608096(G;G)
Significance Probable-Pathogenic
Disease Lynch syndrome
Variation info
Gene MSH6
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000002.11:g.48030825G>A
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000074854.2,