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rs267608147

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs267608147(G;T)
Make rs267608147(T;T)
ReferenceGRCh38 38.1/141
Chromosome7
Position5999107
GenePMS2
is asnp
is mentioned by
dbSNPrs267608147
ebirs267608147
HLIrs267608147
Exacrs267608147
Varsomers267608147
Maprs267608147
PheGenIrs267608147
hapmaprs267608147
1000 genomesrs267608147
hgdprs267608147
ensemblrs267608147
gopubmedrs267608147
geneviewrs267608147
scholarrs267608147
googlers267608147
pharmgkbrs267608147
gwascentralrs267608147
openSNPrs267608147
23andMers267608147
23andMe allrs267608147
SNP Nexus

SNPshotrs267608147
SNPdbers267608147
MSV3drs267608147
GWAS Ctlgrs267608147
Max Magnitude0
ClinVar
Risk rs267608147(T;T)
Alt rs267608147(T;T)
Reference rs267608147(G;G)
Significance Probable-Pathogenic
Disease Lynch syndrome
Variation info
Gene PMS2
CLNDBN Lynch syndrome
Reversed 1
HGVS NC_000007.13:g.6038738C>A
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000076883.2,