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rs587782304

From SNPedia

Orientationplus
Geno Mag Summary
(AAAT;AAAT) 0 common in clinvar
Make rs587782304(-;-)
Make rs587782304(-;AAAT)
ReferenceGRCh38.p2 38.2/144
Chromosome10
Position87961076
GenePTEN
is asnp
is mentioned by
dbSNPrs587782304
ebirs587782304
HLIrs587782304
Exacrs587782304
Varsomers587782304
Maprs587782304
PheGenIrs587782304
hapmaprs587782304
1000 genomesrs587782304
hgdprs587782304
ensemblrs587782304
gopubmedrs587782304
geneviewrs587782304
scholarrs587782304
googlers587782304
pharmgkbrs587782304
gwascentralrs587782304
openSNPrs587782304
23andMers587782304
23andMe allrs587782304
SNP Nexus

SNPshotrs587782304
SNPdbers587782304
MSV3drs587782304
GWAS Ctlgrs587782304
Max Magnitude0
ClinVar
Risk rs587782304(;)
Alt rs587782304(;)
Reference rs587782304(AAAT;AAAT)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome not provided
Variation info
Gene PTEN
CLNDBN Hereditary cancer-predisposing syndrome not provided
Reversed 0
HGVS NC_000010.10:g.89720836_89720839delTAAA
CLNSRC
CLNACC RCV000169834.3, RCV000212887.1,