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rs746930141

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs746930141(C;C)
Make rs746930141(C;G)
ReferenceGRCh38.p2 38.2/144
Chromosome10
Position87961011
GenePTEN
is asnp
is mentioned by
dbSNPrs746930141
ebirs746930141
HLIrs746930141
Exacrs746930141
Varsomers746930141
Maprs746930141
PheGenIrs746930141
hapmaprs746930141
1000 genomesrs746930141
hgdprs746930141
ensemblrs746930141
gopubmedrs746930141
geneviewrs746930141
scholarrs746930141
googlers746930141
pharmgkbrs746930141
gwascentralrs746930141
openSNPrs746930141
23andMers746930141
23andMe allrs746930141
SNP Nexus

SNPshotrs746930141
SNPdbers746930141
MSV3drs746930141
GWAS Ctlgrs746930141
Max Magnitude0
ClinVar
Risk rs746930141(C,T;C,T)
Alt rs746930141(C,T;C,T)
Reference rs746930141(G;G)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome not provided
Variation info
Gene PTEN
CLNDBN Hereditary cancer-predisposing syndrome not provided
Reversed 0
HGVS NC_000010.10:g.89720768G>C; NC_000010.10:g.89720768G>T
CLNSRC
CLNACC RCV000164957.1, RCV000169816.2,