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rs786202786

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(-;G)
(G;G) 0 common in clinvar


Make rs786202786(-;-)
ReferenceGRCh38.p2 38.2/146
Chromosome10
Position87864511
GeneKLLN, PTEN
is asnp
is mentioned by
dbSNPrs786202786
dbSNP (old)rs786202786
ClinGenrs786202786
ebirs786202786
HLIrs786202786
Exacrs786202786
Gnomadrs786202786
Varsomers786202786
Maprs786202786
PheGenIrs786202786
Biobankrs786202786
1000 genomesrs786202786
hgdprs786202786
ensemblrs786202786
gopubmedrs786202786
geneviewrs786202786
scholarrs786202786
googlers786202786
pharmgkbrs786202786
gwascentralrs786202786
openSNPrs786202786
23andMers786202786
23andMe allrs786202786
SNP Nexus

SNPshotrs786202786
SNPdbers786202786
MSV3drs786202786
GWAS Ctlgrs786202786
Max Magnitude0
ClinVar
Risk rs786202786(-;-)
Alt rs786202786(-;-)
Reference Rs786202786(G;G)
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.89624268delG
CLNSRC
CLNACC RCV000165773.1,