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rs587781716

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs587781716(-;-)
Make rs587781716(-;G)
ReferenceGRCh38.p2 38.2/144
Chromosome7
Position6003718
GenePMS2
is asnp
is mentioned by
dbSNPrs587781716
ebirs587781716
HLIrs587781716
Exacrs587781716
Varsomers587781716
Maprs587781716
PheGenIrs587781716
hapmaprs587781716
1000 genomesrs587781716
hgdprs587781716
ensemblrs587781716
gopubmedrs587781716
geneviewrs587781716
scholarrs587781716
googlers587781716
pharmgkbrs587781716
gwascentralrs587781716
openSNPrs587781716
23andMers587781716
23andMe allrs587781716
SNP Nexus

SNPshotrs587781716
SNPdbers587781716
MSV3drs587781716
GWAS Ctlgrs587781716
Max Magnitude0
ClinVar
Risk rs587781716(;)
Alt rs587781716(;)
Reference rs587781716(G;G)
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.6043349delC
CLNSRC
CLNACC RCV000129899.2, RCV000233229.1,