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rs606231170

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs606231170(A;A)
Make rs606231170(A;T)
ReferenceGRCh38.p2 38.2/144
Chromosome10
Position87952189
GenePTEN
is asnp
is mentioned by
dbSNPrs606231170
ebirs606231170
HLIrs606231170
Exacrs606231170
Varsomers606231170
Maprs606231170
PheGenIrs606231170
hapmaprs606231170
1000 genomesrs606231170
hgdprs606231170
ensemblrs606231170
gopubmedrs606231170
geneviewrs606231170
scholarrs606231170
googlers606231170
pharmgkbrs606231170
gwascentralrs606231170
openSNPrs606231170
23andMers606231170
23andMe allrs606231170
SNP Nexus

SNPshotrs606231170
SNPdbers606231170
MSV3drs606231170
GWAS Ctlgrs606231170
Max Magnitude0
ClinVar
Risk rs606231170(A;A)
Alt rs606231170(A;A)
Reference rs606231170(T;T)
Significance Pathogenic
Disease Prostate cancer
Variation info
Gene PTEN
CLNDBN Prostate cancer, somatic
Reversed 0
HGVS NC_000010.10:g.89711946T>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000008277.4,