Have questions? Visit https://www.reddit.com/r/SNPedia

rs587779337

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs587779337(A;A)
Make rs587779337(A;G)
ReferenceGRCh38.p2 38.2/147
Chromosome7
Position5978622
GenePMS2
is asnp
is mentioned by
dbSNPrs587779337
ebirs587779337
HLIrs587779337
Exacrs587779337
Varsomers587779337
Maprs587779337
PheGenIrs587779337
hapmaprs587779337
1000 genomesrs587779337
hgdprs587779337
ensemblrs587779337
gopubmedrs587779337
geneviewrs587779337
scholarrs587779337
googlers587779337
pharmgkbrs587779337
gwascentralrs587779337
openSNPrs587779337
23andMers587779337
23andMe allrs587779337
SNP Nexus

SNPshotrs587779337
SNPdbers587779337
MSV3drs587779337
GWAS Ctlgrs587779337
Max Magnitude0
ClinVar
Risk rs587779337(A;A)
Alt rs587779337(A;A)
Reference rs587779337(G;G)
Significance Probable-Pathogenic
Disease Lynch syndrome Hereditary cancer-predisposing syndrome not specified
Variation info
Gene PMS2
CLNDBN Lynch syndrome Hereditary cancer-predisposing syndrome not specified
Reversed 1
HGVS NC_000007.13:g.6018253C>T
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000076849.2, RCV000115679.5, RCV000212868.1,