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rs587781339

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs587781339(A;G)
Make rs587781339(G;G)
ReferenceGRCh38.p2 38.2/144
Chromosome7
Position5992059
GenePMS2
is asnp
is mentioned by
dbSNPrs587781339
ebirs587781339
HLIrs587781339
Exacrs587781339
Varsomers587781339
Maprs587781339
PheGenIrs587781339
hapmaprs587781339
1000 genomesrs587781339
hgdprs587781339
ensemblrs587781339
gopubmedrs587781339
geneviewrs587781339
scholarrs587781339
googlers587781339
pharmgkbrs587781339
gwascentralrs587781339
openSNPrs587781339
23andMers587781339
23andMe allrs587781339
SNP Nexus

SNPshotrs587781339
SNPdbers587781339
MSV3drs587781339
GWAS Ctlgrs587781339
Max Magnitude0
ClinVar
Risk rs587781339(G;G)
Alt rs587781339(G;G)
Reference rs587781339(A;A)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome Lynch syndrome
Variation info
Gene PMS2
CLNDBN Hereditary cancer-predisposing syndrome Lynch syndrome
Reversed 1
HGVS NC_000007.13:g.6031690T>C
CLNSRC
CLNACC RCV000129110.2, RCV000206112.2,