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rs587780064

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs587780064(G;T)
Make rs587780064(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome7
Position5989956
GenePMS2
is asnp
is mentioned by
dbSNPrs587780064
ebirs587780064
HLIrs587780064
Exacrs587780064
Varsomers587780064
Maprs587780064
PheGenIrs587780064
hapmaprs587780064
1000 genomesrs587780064
hgdprs587780064
ensemblrs587780064
gopubmedrs587780064
geneviewrs587780064
scholarrs587780064
googlers587780064
pharmgkbrs587780064
gwascentralrs587780064
openSNPrs587780064
23andMers587780064
23andMe allrs587780064
SNP Nexus

SNPshotrs587780064
SNPdbers587780064
MSV3drs587780064
GWAS Ctlgrs587780064
Max Magnitude0
ClinVar
Risk rs587780064(T;T)
Alt rs587780064(T;T)
Reference rs587780064(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene PMS2
CLNDBN not provided
Reversed 1
HGVS NC_000007.13:g.6029587C>A
CLNSRC
CLNACC RCV000115713.2,