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rs267608036

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs267608036(A;A)
Make rs267608036(A;T)
ReferenceGRCh38 38.1/141
Chromosome2
Position47791125
GeneMSH6
is asnp
is mentioned by
dbSNPrs267608036
dbSNP (old)rs267608036
ClinGenrs267608036
ebirs267608036
HLIrs267608036
Exacrs267608036
Gnomadrs267608036
Varsomers267608036
Maprs267608036
PheGenIrs267608036
Biobankrs267608036
1000 genomesrs267608036
hgdprs267608036
ensemblrs267608036
gopubmedrs267608036
geneviewrs267608036
scholarrs267608036
googlers267608036
pharmgkbrs267608036
gwascentralrs267608036
openSNPrs267608036
23andMers267608036
23andMe allrs267608036
SNP Nexus

SNPshotrs267608036
SNPdbers267608036
MSV3drs267608036
GWAS Ctlgrs267608036
Max Magnitude0
ClinVar
Risk rs267608036(A;A)
Alt rs267608036(A;A)
Reference Rs267608036(T;T)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MSH6
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000002.11:g.48018264T>A
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000074993.2,