Have questions? Visit https://www.reddit.com/r/SNPedia

rs375709098

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs375709098(C;T)
Make rs375709098(T;T)
ReferenceGRCh38 38.1/142
Chromosome10
Position87965321
GenePTEN
is asnp
is mentioned by
dbSNPrs375709098
ebirs375709098
HLIrs375709098
Exacrs375709098
Varsomers375709098
Maprs375709098
PheGenIrs375709098
hapmaprs375709098
1000 genomesrs375709098
hgdprs375709098
ensemblrs375709098
gopubmedrs375709098
geneviewrs375709098
scholarrs375709098
googlers375709098
pharmgkbrs375709098
gwascentralrs375709098
openSNPrs375709098
23andMers375709098
23andMe allrs375709098
SNP Nexus

SNPshotrs375709098
SNPdbers375709098
MSV3drs375709098
GWAS Ctlgrs375709098
Max Magnitude0
ClinVar
Risk rs375709098(A,T;A,T)
Alt rs375709098(A,T;A,T)
Reference rs375709098(C;C)
Significance Probable-Pathogenic
Disease Tumor susceptibility linked to germline BAP1 mutations not specified PTEN hamartoma tumor syndrome Inborn genetic diseases Hereditary cancer-predisposing syndrome not provided
Variation info
Gene PTEN
CLNDBN Tumor susceptibility linked to germline BAP1 mutations not specified PTEN hamartoma tumor syndrome Inborn genetic diseases Hereditary cancer-predisposing syndrome not provided
Reversed 0
HGVS NC_000010.10:g.89725078C>A; NC_000010.10:g.89725078C>T
CLNSRC Ambry Genetics ClinVar
CLNACC RCV000132539.4, RCV000201314.2, RCV000205690.1, RCV000210607.1, RCV000131204.2, RCV000180490.1,