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rs587779324

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs587779324(A;G)
Make rs587779324(G;G)
ReferenceGRCh38.p2 38.2/144
Chromosome7
Position6004060
GenePMS2
is asnp
is mentioned by
dbSNPrs587779324
ebirs587779324
HLIrs587779324
Exacrs587779324
Varsomers587779324
Maprs587779324
PheGenIrs587779324
hapmaprs587779324
1000 genomesrs587779324
hgdprs587779324
ensemblrs587779324
gopubmedrs587779324
geneviewrs587779324
scholarrs587779324
googlers587779324
pharmgkbrs587779324
gwascentralrs587779324
openSNPrs587779324
23andMers587779324
23andMe allrs587779324
SNP Nexus

SNPshotrs587779324
SNPdbers587779324
MSV3drs587779324
GWAS Ctlgrs587779324
Max Magnitude0
ClinVar
Risk rs587779324(G;G)
Alt rs587779324(G;G)
Reference rs587779324(A;A)
Significance Probable-Pathogenic
Disease Lynch syndrome
Variation info
Gene PMS2
CLNDBN Lynch syndrome
Reversed 1
HGVS NC_000007.13:g.6043691T>C
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000076818.2,