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rs786201041

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs786201041(A;A)
Make rs786201041(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome10
Position87961119
GenePTEN
is asnp
is mentioned by
dbSNPrs786201041
ebirs786201041
HLIrs786201041
Exacrs786201041
Varsomers786201041
Maprs786201041
PheGenIrs786201041
hapmaprs786201041
1000 genomesrs786201041
hgdprs786201041
ensemblrs786201041
gopubmedrs786201041
geneviewrs786201041
scholarrs786201041
googlers786201041
pharmgkbrs786201041
gwascentralrs786201041
openSNPrs786201041
23andMers786201041
23andMe allrs786201041
SNP Nexus

SNPshotrs786201041
SNPdbers786201041
MSV3drs786201041
GWAS Ctlgrs786201041
Max Magnitude0
ClinVar
Risk rs786201041(A,C;A,C)
Alt rs786201041(A,C;A,C)
Reference rs786201041(G;G)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene PTEN
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000010.10:g.89720876G>A; NC_000010.10:g.89720876G>C
CLNSRC
CLNACC RCV000162423.1, RCV000169898.1,