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rs786204882

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(-;GATCGTTAGCAGAAACA) 6.3 Hereditary cancer predisposing syndrome
(AGATCGTTAGCAGAAAC;AGATCGTTAGCAGAAAC) 0 common in clinvar
(GATCGTTAGCAGAAACA;GATCGTTAGCAGAAACA) 0 common/normal


Make rs786204882(-;-)
ReferenceGRCh38.p2 38.2/146
Chromosome10
Position87864490
GeneKLLN, PTEN
is asnp
is mentioned by
dbSNPrs786204882
dbSNP (old)rs786204882
ClinGenrs786204882
ebirs786204882
HLIrs786204882
Exacrs786204882
Varsomers786204882
Maprs786204882
PheGenIrs786204882
Biobankrs786204882
1000 genomesrs786204882
hgdprs786204882
ensemblrs786204882
gopubmedrs786204882
geneviewrs786204882
scholarrs786204882
googlers786204882
pharmgkbrs786204882
gwascentralrs786204882
openSNPrs786204882
23andMers786204882
23andMe allrs786204882
SNP Nexus

SNPshotrs786204882
SNPdbers786204882
MSV3drs786204882
GWAS Ctlgrs786204882
Max Magnitude6.3
ClinVar
Risk rs786204882(-;-)
Alt rs786204882(-;-)
Reference Rs786204882(AGATCGTTAGCAGAAAC;AGATCGTTAGCAGAAAC)
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.89624247_89624263del17
CLNSRC
CLNACC RCV000169823.1,