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rs786204900

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs786204900(-;-)
Make rs786204900(-;A)
ReferenceGRCh38.p2 38.2/146
Chromosome10
Position87933250
GenePTEN
is asnp
is mentioned by
dbSNPrs786204900
ebirs786204900
HLIrs786204900
Exacrs786204900
Varsomers786204900
Maprs786204900
PheGenIrs786204900
hapmaprs786204900
1000 genomesrs786204900
hgdprs786204900
ensemblrs786204900
gopubmedrs786204900
geneviewrs786204900
scholarrs786204900
googlers786204900
pharmgkbrs786204900
gwascentralrs786204900
openSNPrs786204900
23andMers786204900
23andMe allrs786204900
SNP Nexus

SNPshotrs786204900
SNPdbers786204900
MSV3drs786204900
GWAS Ctlgrs786204900
Max Magnitude0
ClinVar
Risk rs786204900(;)
Alt rs786204900(;)
Reference rs786204900(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.89693007delA
CLNSRC
CLNACC RCV000169841.1,