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rs587781255

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs587781255(A;A)
Make rs587781255(A;G)
ReferenceGRCh38.p2 38.2/144
Chromosome10
Position87933138
GenePTEN
is asnp
is mentioned by
dbSNPrs587781255
ebirs587781255
HLIrs587781255
Exacrs587781255
Varsomers587781255
Maprs587781255
PheGenIrs587781255
hapmaprs587781255
1000 genomesrs587781255
hgdprs587781255
ensemblrs587781255
gopubmedrs587781255
geneviewrs587781255
scholarrs587781255
googlers587781255
pharmgkbrs587781255
gwascentralrs587781255
openSNPrs587781255
23andMers587781255
23andMe allrs587781255
SNP Nexus

SNPshotrs587781255
SNPdbers587781255
MSV3drs587781255
GWAS Ctlgrs587781255
Max Magnitude0
ClinVar
Risk rs587781255(A;A)
Alt rs587781255(A;A)
Reference rs587781255(G;G)
Significance Pathogenic
Disease PTEN hamartoma tumor syndrome
Variation info
Gene PTEN
CLNDBN PTEN hamartoma tumor syndrome
Reversed 0
HGVS NC_000010.10:g.89692895G>A
CLNSRC
CLNACC RCV000128454.1,