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rs786201995

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs786201995(A;A)
Make rs786201995(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome10
Position87864539
GeneKLLN, PTEN
is asnp
is mentioned by
dbSNPrs786201995
ebirs786201995
HLIrs786201995
Exacrs786201995
Varsomers786201995
Maprs786201995
PheGenIrs786201995
hapmaprs786201995
1000 genomesrs786201995
hgdprs786201995
ensemblrs786201995
gopubmedrs786201995
geneviewrs786201995
scholarrs786201995
googlers786201995
pharmgkbrs786201995
gwascentralrs786201995
openSNPrs786201995
23andMers786201995
23andMe allrs786201995
SNP Nexus

SNPshotrs786201995
SNPdbers786201995
MSV3drs786201995
GWAS Ctlgrs786201995
Max Magnitude0
ClinVar
Risk rs786201995(A,C,T;A,C,T)
Alt rs786201995(A,C,T;A,C,T)
Reference rs786201995(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.89624296G>A; NC_000010.10:g.89624296G>C; NC_000010.10:g.89624296G>T
CLNSRC
CLNACC RCV000164570.1, RCV000165524.1, RCV000169787.1,