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rs267608156

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(;) 0 common in clinvar
Make rs267608156(-;-)
Make rs267608156(-;T)
Make rs267608156(T;T)
ReferenceGRCh38 38.1/141
Chromosome7
Position5989867
GenePMS2
is asnp
is mentioned by
dbSNPrs267608156
ebirs267608156
HLIrs267608156
Exacrs267608156
Varsomers267608156
Maprs267608156
PheGenIrs267608156
hapmaprs267608156
1000 genomesrs267608156
hgdprs267608156
ensemblrs267608156
gopubmedrs267608156
geneviewrs267608156
scholarrs267608156
googlers267608156
pharmgkbrs267608156
gwascentralrs267608156
openSNPrs267608156
23andMers267608156
23andMe allrs267608156
SNP Nexus

SNPshotrs267608156
SNPdbers267608156
MSV3drs267608156
GWAS Ctlgrs267608156
Max Magnitude0
ClinVar
Risk rs267608156(T;T)
Alt rs267608156(T;T)
Reference rs267608156(;)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene PMS2
CLNDBN Lynch syndrome
Reversed 1
HGVS NC_000007.13:g.6029499dupA
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000076794.2,