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rs267608006

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs267608006(A;A)
Make rs267608006(A;T)
ReferenceGRCh38.p7 38.3/150
Chromosome2
Position47478262
GeneMSH2
is asnp
is mentioned by
dbSNPrs267608006
dbSNP (old)rs267608006
ClinGenrs267608006
ebirs267608006
HLIrs267608006
Exacrs267608006
Gnomadrs267608006
Varsomers267608006
Maprs267608006
PheGenIrs267608006
Biobankrs267608006
1000 genomesrs267608006
hgdprs267608006
ensemblrs267608006
gopubmedrs267608006
geneviewrs267608006
scholarrs267608006
googlers267608006
pharmgkbrs267608006
gwascentralrs267608006
openSNPrs267608006
23andMers267608006
23andMe allrs267608006
SNPshotrs267608006
SNPdbers267608006
MSV3drs267608006
GWAS Ctlgrs267608006
Max Magnitude0
ClinVar
Risk rs267608006(A;A)
Alt rs267608006(A;A)
Reference Rs267608006(T;T)
Significance Probable-Pathogenic
Disease Lynch syndrome not specified Hereditary cancer-predisposing syndrome
Variation info
Gene MSH2
CLNDBN Lynch syndrome not specified Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000002.11:g.47705401T>A
CLNSRC
CLNACC RCV000076429.2, RCV000478566.1, RCV000491555.1,