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rs876660507

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs876660507(G;T)
Make rs876660507(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome10
Position87952134
GenePTEN
is asnp
is mentioned by
dbSNPrs876660507
ebirs876660507
HLIrs876660507
Exacrs876660507
Varsomers876660507
Maprs876660507
PheGenIrs876660507
hapmaprs876660507
1000 genomesrs876660507
hgdprs876660507
ensemblrs876660507
gopubmedrs876660507
geneviewrs876660507
scholarrs876660507
googlers876660507
pharmgkbrs876660507
gwascentralrs876660507
openSNPrs876660507
23andMers876660507
23andMe allrs876660507
SNP Nexus

SNPshotrs876660507
SNPdbers876660507
MSV3drs876660507
GWAS Ctlgrs876660507
Max Magnitude0
ClinVar
Risk rs876660507(T;T)
Alt rs876660507(T;T)
Reference rs876660507(G;G)
Significance 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.89711891G>T
CLNSRC
CLNACC RCV000217155.1,