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rs786204883

From SNPedia

Orientationplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs786204883(-;-)
Make rs786204883(-;T)
Make rs786204883(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome10
Position87864515
GeneKLLN, PTEN
is asnp
is mentioned by
dbSNPrs786204883
ebirs786204883
HLIrs786204883
Exacrs786204883
Varsomers786204883
Maprs786204883
PheGenIrs786204883
hapmaprs786204883
1000 genomesrs786204883
hgdprs786204883
ensemblrs786204883
gopubmedrs786204883
geneviewrs786204883
scholarrs786204883
googlers786204883
pharmgkbrs786204883
gwascentralrs786204883
openSNPrs786204883
23andMers786204883
23andMe allrs786204883
SNP Nexus

SNPshotrs786204883
SNPdbers786204883
MSV3drs786204883
GWAS Ctlgrs786204883
Max Magnitude0
ClinVar
Risk rs786204883(T;T)
Alt rs786204883(T;T)
Reference rs786204883(;)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene PTEN LOC101929706 KLLN
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000010.10:g.89624272dupT
CLNSRC
CLNACC RCV000169824.1,