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rs1057520622

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common/normal
(A;T) 6.3 Hereditary cancer predisposing syndrome
Make rs1057520622(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome10
Position87933189
GenePTEN
is asnp
is mentioned by
dbSNPrs1057520622
dbSNP (old)rs1057520622
ClinGenrs1057520622
ebirs1057520622
HLIrs1057520622
Exacrs1057520622
Gnomadrs1057520622
Varsomers1057520622
Maprs1057520622
PheGenIrs1057520622
Biobankrs1057520622
1000 genomesrs1057520622
hgdprs1057520622
ensemblrs1057520622
gopubmedrs1057520622
geneviewrs1057520622
scholarrs1057520622
googlers1057520622
pharmgkbrs1057520622
gwascentralrs1057520622
openSNPrs1057520622
23andMers1057520622
23andMe allrs1057520622
SNPshotrs1057520622
SNPdbers1057520622
MSV3drs1057520622
GWAS Ctlgrs1057520622
Max Magnitude6.3
ClinVar
Risk rs1057520622(T;T)
Alt rs1057520622(T;T)
Reference Rs1057520622(A;A)
Significance Pathogenic
Disease not provided
Variation info
Gene PTEN
CLNDBN not provided
Reversed 0
HGVS NC_000010.10:g.89692946A>T
CLNSRC
CLNACC RCV000435296.1,