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rs786201039

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs786201039(G;T)
Make rs786201039(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome7
Position5973482
GenePMS2
is asnp
is mentioned by
dbSNPrs786201039
ebirs786201039
HLIrs786201039
Exacrs786201039
Varsomers786201039
Maprs786201039
PheGenIrs786201039
hapmaprs786201039
1000 genomesrs786201039
hgdprs786201039
ensemblrs786201039
gopubmedrs786201039
geneviewrs786201039
scholarrs786201039
googlers786201039
pharmgkbrs786201039
gwascentralrs786201039
openSNPrs786201039
23andMers786201039
23andMe allrs786201039
SNP Nexus

SNPshotrs786201039
SNPdbers786201039
MSV3drs786201039
GWAS Ctlgrs786201039
Max Magnitude0
ClinVar
Risk rs786201039(T;T)
Alt rs786201039(T;T)
Reference rs786201039(G;G)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene PMS2
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 1
HGVS NC_000007.13:g.6013113C>A
CLNSRC
CLNACC RCV000162416.1,