Have questions? Visit https://www.reddit.com/r/SNPedia

rs606231169

From SNPedia

Orientationplus
Geno Mag Summary
(AAAGT;AAAGT) 0 common in clinvar
Make rs606231169(-;-)
Make rs606231169(-;AAGTA)
Make rs606231169(AAGTA;AAGTA)
ReferenceGRCh38.p2 38.2/144
Chromosome10
Position87957979
GenePTEN
is asnp
is mentioned by
dbSNPrs606231169
ebirs606231169
HLIrs606231169
Exacrs606231169
Varsomers606231169
Maprs606231169
PheGenIrs606231169
hapmaprs606231169
1000 genomesrs606231169
hgdprs606231169
ensemblrs606231169
gopubmedrs606231169
geneviewrs606231169
scholarrs606231169
googlers606231169
pharmgkbrs606231169
gwascentralrs606231169
openSNPrs606231169
23andMers606231169
23andMe allrs606231169
SNP Nexus

SNPshotrs606231169
SNPdbers606231169
MSV3drs606231169
GWAS Ctlgrs606231169
Max Magnitude0
ClinVar
Risk rs606231169(;)
Alt rs606231169(;)
Reference rs606231169(AAAGT;AAAGT)
Significance Pathogenic
Disease Prostate cancer
Variation info
Gene PTEN
CLNDBN Prostate cancer, somatic
Reversed 0
HGVS NC_000010.10:g.89717736_89717740delAAGTA
CLNSRC OMIM Allelic Variant
CLNACC RCV000008276.4,