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rs786204863

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs786204863(G;T)
Make rs786204863(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome10
Position87952119
GenePTEN
is asnp
is mentioned by
dbSNPrs786204863
ebirs786204863
HLIrs786204863
Exacrs786204863
Varsomers786204863
Maprs786204863
PheGenIrs786204863
hapmaprs786204863
1000 genomesrs786204863
hgdprs786204863
ensemblrs786204863
gopubmedrs786204863
geneviewrs786204863
scholarrs786204863
googlers786204863
pharmgkbrs786204863
gwascentralrs786204863
openSNPrs786204863
23andMers786204863
23andMe allrs786204863
SNP Nexus

SNPshotrs786204863
SNPdbers786204863
MSV3drs786204863
GWAS Ctlgrs786204863
Max Magnitude0
ClinVar
Risk rs786204863(T;T)
Alt rs786204863(T;T)
Reference rs786204863(G;G)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene PTEN
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000010.10:g.89711876G>T
CLNSRC
CLNACC RCV000169803.1,