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rs746128825

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs746128825(A;A)
Make rs746128825(A;T)
ReferenceGRCh38.p2 38.2/144
Chromosome10
Position87864548
GeneKLLN, PTEN
is asnp
is mentioned by
dbSNPrs746128825
ebirs746128825
HLIrs746128825
Exacrs746128825
Varsomers746128825
Maprs746128825
PheGenIrs746128825
hapmaprs746128825
1000 genomesrs746128825
hgdprs746128825
ensemblrs746128825
gopubmedrs746128825
geneviewrs746128825
scholarrs746128825
googlers746128825
pharmgkbrs746128825
gwascentralrs746128825
openSNPrs746128825
23andMers746128825
23andMe allrs746128825
SNP Nexus

SNPshotrs746128825
SNPdbers746128825
MSV3drs746128825
GWAS Ctlgrs746128825
Max Magnitude0
ClinVar
Risk rs746128825(A;A)
Alt rs746128825(A;A)
Reference rs746128825(T;T)
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.89624305T>A
CLNSRC
CLNACC RCV000169852.1,