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rs767623493

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs767623493(C;C)
Make rs767623493(C;T)
ReferenceGRCh38.p2 38.2/147
Chromosome10
Position87957968
GenePTEN
is asnp
is mentioned by
dbSNPrs767623493
ebirs767623493
HLIrs767623493
Exacrs767623493
Varsomers767623493
Maprs767623493
PheGenIrs767623493
hapmaprs767623493
1000 genomesrs767623493
hgdprs767623493
ensemblrs767623493
gopubmedrs767623493
geneviewrs767623493
scholarrs767623493
googlers767623493
pharmgkbrs767623493
gwascentralrs767623493
openSNPrs767623493
23andMers767623493
23andMe allrs767623493
SNP Nexus

SNPshotrs767623493
SNPdbers767623493
MSV3drs767623493
GWAS Ctlgrs767623493
Max Magnitude0
ClinVar
Risk rs767623493(C;C)
Alt rs767623493(C;C)
Reference rs767623493(T;T)
Significance Pathogenic
Disease Tumor susceptibility linked to germline BAP1 mutations Hereditary cancer-predisposing syndrome
Variation info
Gene PTEN
CLNDBN Tumor susceptibility linked to germline BAP1 mutations Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000010.10:g.89717725T>A; NC_000010.10:g.89717725T>C
CLNSRC
CLNACC RCV000218967.1, RCV000164253.1,