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rs786201062

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs786201062(-;-)
Make rs786201062(-;A)
ReferenceGRCh38.p2 38.2/146
Chromosome7
Position5982842
GenePMS2
is asnp
is mentioned by
dbSNPrs786201062
ebirs786201062
HLIrs786201062
Exacrs786201062
Varsomers786201062
Maprs786201062
PheGenIrs786201062
hapmaprs786201062
1000 genomesrs786201062
hgdprs786201062
ensemblrs786201062
gopubmedrs786201062
geneviewrs786201062
scholarrs786201062
googlers786201062
pharmgkbrs786201062
gwascentralrs786201062
openSNPrs786201062
23andMers786201062
23andMe allrs786201062
SNP Nexus

SNPshotrs786201062
SNPdbers786201062
MSV3drs786201062
GWAS Ctlgrs786201062
Max Magnitude0
ClinVar
Risk rs786201062(;)
Alt rs786201062(;)
Reference rs786201062(A;A)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene PMS2
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 1
HGVS NC_000007.13:g.6022473delT
CLNSRC
CLNACC RCV000162471.1,