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

rs786204865

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs786204865(A;G)
Make rs786204865(G;G)
ReferenceGRCh38.p2 38.2/146
Chromosome10
Position87952137
GenePTEN
is asnp
is mentioned by
dbSNPrs786204865
ebirs786204865
HLIrs786204865
Exacrs786204865
Varsomers786204865
Maprs786204865
PheGenIrs786204865
hapmaprs786204865
1000 genomesrs786204865
hgdprs786204865
ensemblrs786204865
gopubmedrs786204865
geneviewrs786204865
scholarrs786204865
googlers786204865
pharmgkbrs786204865
gwascentralrs786204865
openSNPrs786204865
23andMers786204865
23andMe allrs786204865
SNP Nexus

SNPshotrs786204865
SNPdbers786204865
MSV3drs786204865
GWAS Ctlgrs786204865
Max Magnitude0
ClinVar
Risk rs786204865(G;G)
Alt rs786204865(G;G)
Reference rs786204865(A;A)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene PTEN
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000010.10:g.89711894A>G
CLNSRC
CLNACC RCV000169805.1,