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rs786204885

From SNPedia

Merged intors587781340
Orientationplus
Stabilizedplus
Geno Mag Summary
(GCAAAAGCCGCA;GCAAAAGCCGCA) 0 common in clinvar
Make rs786204885(-;-)
Make rs786204885(-;AAGCCGCAGCAA)
Make rs786204885(AAGCCGCAGCAA;AAGCCGCAGCAA)
ReferenceGRCh38.p2 38.2/146
Chromosome10
Position87863274
GeneKLLN, PTEN
is asnp
is mentioned by
dbSNPrs786204885
dbSNP (old)rs786204885
ClinGenrs786204885
ebirs786204885
HLIrs786204885
Exacrs786204885
Varsomers786204885
Maprs786204885
PheGenIrs786204885
Biobankrs786204885
1000 genomesrs786204885
hgdprs786204885
ensemblrs786204885
gopubmedrs786204885
geneviewrs786204885
scholarrs786204885
googlers786204885
pharmgkbrs786204885
gwascentralrs786204885
openSNPrs786204885
23andMers786204885
23andMe allrs786204885
SNP Nexus

SNPshotrs786204885
SNPdbers786204885
MSV3drs786204885
GWAS Ctlgrs786204885
StatusMerged into rs587781340
Max Magnitude0
ClinVar
Risk
Alt
Reference Rs786204885(GCAAAAGCCGCA;GCAAAAGCCGCA)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome not specified
Variation info
Gene PTEN LOC101929706 KLLN
CLNDBN Hereditary cancer-predisposing syndrome not specified
Reversed 0
HGVS NC_000010.10:g.89623031_89623042delAAGCCGCAGCAA
CLNSRC GeneDx
CLNACC RCV000129113.4, RCV000169826.2,