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rs786204910

From SNPedia

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Geno Mag Summary
(C;C) 0 common in clinvar
Make rs786204910(C;T)
Make rs786204910(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome10
Position87864518
GeneKLLN, PTEN
is asnp
is mentioned by
dbSNPrs786204910
ebirs786204910
HLIrs786204910
Exacrs786204910
Varsomers786204910
Maprs786204910
PheGenIrs786204910
hapmaprs786204910
1000 genomesrs786204910
hgdprs786204910
ensemblrs786204910
gopubmedrs786204910
geneviewrs786204910
scholarrs786204910
googlers786204910
pharmgkbrs786204910
gwascentralrs786204910
openSNPrs786204910
23andMers786204910
23andMe allrs786204910
SNP Nexus

SNPshotrs786204910
SNPdbers786204910
MSV3drs786204910
GWAS Ctlgrs786204910
Max Magnitude0
ClinVar
Risk rs786204910(T;T)
Alt rs786204910(T;T)
Reference rs786204910(C;C)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome PTEN hamartoma tumor syndrome Tumor susceptibility linked to germline BAP1 mutations
Variation info
Gene PTEN LOC101929706 KLLN
CLNDBN Hereditary cancer-predisposing syndrome PTEN hamartoma tumor syndrome Tumor susceptibility linked to germline BAP1 mutations
Reversed 0
HGVS NC_000010.10:g.89624275C>T
CLNSRC
CLNACC RCV000169851.1, RCV000204017.1, RCV000220466.1,