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

rs371387815

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs371387815(C;G)
Make rs371387815(G;G)
ReferenceGRCh38.p2 38.2/144
Chromosome10
Position87960984
GenePTEN
is asnp
is mentioned by
dbSNPrs371387815
ebirs371387815
HLIrs371387815
Exacrs371387815
Varsomers371387815
Maprs371387815
PheGenIrs371387815
hapmaprs371387815
1000 genomesrs371387815
hgdprs371387815
ensemblrs371387815
gopubmedrs371387815
geneviewrs371387815
scholarrs371387815
googlers371387815
pharmgkbrs371387815
gwascentralrs371387815
openSNPrs371387815
23andMers371387815
23andMe allrs371387815
SNP Nexus

SNPshotrs371387815
SNPdbers371387815
MSV3drs371387815
GWAS Ctlgrs371387815
Max Magnitude0
ClinVar
Risk rs371387815(G,T;G,T)
Alt rs371387815(G,T;G,T)
Reference rs371387815(C;C)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome Cowden syndrome 1 PTEN hamartoma tumor syndrome not specified
Variation info
Gene PTEN
CLNDBN Hereditary cancer-predisposing syndrome Cowden syndrome 1 PTEN hamartoma tumor syndrome not specified
Reversed 0
HGVS NC_000010.10:g.89720741C>G; NC_000010.10:g.89720741C>T
CLNSRC
CLNACC RCV000115590.5, RCV000148765.1, RCV000199677.1, RCV000212885.1, RCV000167405.1,