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rs786204893

From SNPedia

Orientationplus
Geno Mag Summary
(AAAT;AAAT) 0 common in clinvar
Make rs786204893(-;-)
Make rs786204893(-;TAAA)
Make rs786204893(TAAA;TAAA)
ReferenceGRCh38.p2 38.2/146
Chromosome10
Position87961079
GenePTEN
is asnp
is mentioned by
dbSNPrs786204893
ebirs786204893
HLIrs786204893
Exacrs786204893
Varsomers786204893
Maprs786204893
PheGenIrs786204893
hapmaprs786204893
1000 genomesrs786204893
hgdprs786204893
ensemblrs786204893
gopubmedrs786204893
geneviewrs786204893
scholarrs786204893
googlers786204893
pharmgkbrs786204893
gwascentralrs786204893
openSNPrs786204893
23andMers786204893
23andMe allrs786204893
SNP Nexus

SNPshotrs786204893
SNPdbers786204893
MSV3drs786204893
GWAS Ctlgrs786204893
Max Magnitude0
ClinVar
Risk rs786204893(;)
Alt rs786204893(;)
Reference rs786204893(AAAT;AAAT)
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.89720836_89720839delTAAA
CLNSRC
CLNACC RCV000169834.3, RCV000212887.1,