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rs267608149

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(;) 0 common in clinvar
Make rs267608149(-;-)
Make rs267608149(-;T)
Make rs267608149(T;T)
ReferenceGRCh38 38.1/141
Chromosome7
Position5997326
GenePMS2
is asnp
is mentioned by
dbSNPrs267608149
ebirs267608149
HLIrs267608149
Exacrs267608149
Varsomers267608149
Maprs267608149
PheGenIrs267608149
hapmaprs267608149
1000 genomesrs267608149
hgdprs267608149
ensemblrs267608149
gopubmedrs267608149
geneviewrs267608149
scholarrs267608149
googlers267608149
pharmgkbrs267608149
gwascentralrs267608149
openSNPrs267608149
23andMers267608149
23andMe allrs267608149
SNP Nexus

SNPshotrs267608149
SNPdbers267608149
MSV3drs267608149
GWAS Ctlgrs267608149
Max Magnitude0
ClinVar
Risk rs267608149(T;T)
Alt rs267608149(T;T)
Reference rs267608149(;)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene PMS2
CLNDBN Lynch syndrome
Reversed 1
HGVS NC_000007.13:g.6036958dupA
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000076888.2,