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rs587780004

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs587780004(C;T)
Make rs587780004(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome10
Position87894057
GenePTEN
is asnp
is mentioned by
dbSNPrs587780004
ebirs587780004
HLIrs587780004
Exacrs587780004
Varsomers587780004
Maprs587780004
PheGenIrs587780004
hapmaprs587780004
1000 genomesrs587780004
hgdprs587780004
ensemblrs587780004
gopubmedrs587780004
geneviewrs587780004
scholarrs587780004
googlers587780004
pharmgkbrs587780004
gwascentralrs587780004
openSNPrs587780004
23andMers587780004
23andMe allrs587780004
SNP Nexus

SNPshotrs587780004
SNPdbers587780004
MSV3drs587780004
GWAS Ctlgrs587780004
Max Magnitude0
ClinVar
Risk rs587780004(T;T)
Alt rs587780004(T;T)
Reference rs587780004(C;C)
Significance Probable-Pathogenic
Disease Tumor susceptibility linked to germline BAP1 mutations
Variation info
Gene PTEN
CLNDBN Tumor susceptibility linked to germline BAP1 mutations
Reversed 0
HGVS NC_000010.10:g.89653814C>A
CLNSRC
CLNACC RCV000214093.1,