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rs267608148

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(;) 0 common in clinvar
Make rs267608148(-;-)
Make rs267608148(-;T)
Make rs267608148(T;T)
ReferenceGRCh38 38.1/141
Chromosome7
Position5999219
GenePMS2
is asnp
is mentioned by
dbSNPrs267608148
ebirs267608148
HLIrs267608148
Exacrs267608148
Varsomers267608148
Maprs267608148
PheGenIrs267608148
hapmaprs267608148
1000 genomesrs267608148
hgdprs267608148
ensemblrs267608148
gopubmedrs267608148
geneviewrs267608148
scholarrs267608148
googlers267608148
pharmgkbrs267608148
gwascentralrs267608148
openSNPrs267608148
23andMers267608148
23andMe allrs267608148
SNP Nexus

SNPshotrs267608148
SNPdbers267608148
MSV3drs267608148
GWAS Ctlgrs267608148
Max Magnitude0
ClinVar
Risk rs267608148(T;T)
Alt rs267608148(T;T)
Reference rs267608148(;)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene PMS2
CLNDBN Lynch syndrome
Reversed 1
HGVS NC_000007.13:g.6038851dupA
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000076878.2,