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rs1057518425

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1057518425(A;A)
Make rs1057518425(A;G)
ReferenceGRCh38.p7 38.3/150
Chromosome10
Position87894085
GenePTEN
is asnp
is mentioned by
dbSNPrs1057518425
dbSNP (old)rs1057518425
ClinGenrs1057518425
ebirs1057518425
HLIrs1057518425
Exacrs1057518425
Gnomadrs1057518425
Varsomers1057518425
Maprs1057518425
PheGenIrs1057518425
Biobankrs1057518425
1000 genomesrs1057518425
hgdprs1057518425
ensemblrs1057518425
gopubmedrs1057518425
geneviewrs1057518425
scholarrs1057518425
googlers1057518425
pharmgkbrs1057518425
gwascentralrs1057518425
openSNPrs1057518425
23andMers1057518425
23andMe allrs1057518425
SNPshotrs1057518425
SNPdbers1057518425
MSV3drs1057518425
GWAS Ctlgrs1057518425
Max Magnitude0
ClinVar
Risk rs1057518425(A;A)
Alt rs1057518425(A;A)
Reference Rs1057518425(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene PTEN
CLNDBN not provided
Reversed 0
HGVS NC_000010.10:g.89653842G>A
CLNSRC
CLNACC RCV000412756.1,