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rs587781395

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs587781395(-;-)
Make rs587781395(-;A)
ReferenceGRCh38.p2 38.2/144
Chromosome7
Position5989877
GenePMS2
is asnp
is mentioned by
dbSNPrs587781395
ebirs587781395
HLIrs587781395
Exacrs587781395
Varsomers587781395
Maprs587781395
PheGenIrs587781395
hapmaprs587781395
1000 genomesrs587781395
hgdprs587781395
ensemblrs587781395
gopubmedrs587781395
geneviewrs587781395
scholarrs587781395
googlers587781395
pharmgkbrs587781395
gwascentralrs587781395
openSNPrs587781395
23andMers587781395
23andMe allrs587781395
SNP Nexus

SNPshotrs587781395
SNPdbers587781395
MSV3drs587781395
GWAS Ctlgrs587781395
Max Magnitude0
ClinVar
Risk rs587781395(;)
Alt rs587781395(;)
Reference rs587781395(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.6029508delT
CLNSRC
CLNACC RCV000129239.2,