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rs587780724

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs587780724(A;A)
Make rs587780724(A;C)
ReferenceGRCh38.p2 38.2/144
Chromosome7
Position5987389
GenePMS2
is asnp
is mentioned by
dbSNPrs587780724
ebirs587780724
HLIrs587780724
Exacrs587780724
Varsomers587780724
Maprs587780724
PheGenIrs587780724
hapmaprs587780724
1000 genomesrs587780724
hgdprs587780724
ensemblrs587780724
gopubmedrs587780724
geneviewrs587780724
scholarrs587780724
googlers587780724
pharmgkbrs587780724
gwascentralrs587780724
openSNPrs587780724
23andMers587780724
23andMe allrs587780724
SNP Nexus

SNPshotrs587780724
SNPdbers587780724
MSV3drs587780724
GWAS Ctlgrs587780724
Max Magnitude0
ClinVar
Risk rs587780724(A;A)
Alt rs587780724(A;A)
Reference rs587780724(C;C)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene PMS2
CLNDBN Lynch syndrome
Reversed 1
HGVS NC_000007.13:g.6027020G>T
CLNSRC
CLNACC RCV000123077.1,