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rs786202004

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs786202004(A;T)
Make rs786202004(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome10
Position87961056
GenePTEN
is asnp
is mentioned by
dbSNPrs786202004
ebirs786202004
HLIrs786202004
Exacrs786202004
Varsomers786202004
Maprs786202004
PheGenIrs786202004
hapmaprs786202004
1000 genomesrs786202004
hgdprs786202004
ensemblrs786202004
gopubmedrs786202004
geneviewrs786202004
scholarrs786202004
googlers786202004
pharmgkbrs786202004
gwascentralrs786202004
openSNPrs786202004
23andMers786202004
23andMe allrs786202004
SNP Nexus

SNPshotrs786202004
SNPdbers786202004
MSV3drs786202004
GWAS Ctlgrs786202004
Max Magnitude0
ClinVar
Risk rs786202004(T;T)
Alt rs786202004(T;T)
Reference rs786202004(A;A)
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.89720813A>T
CLNSRC
CLNACC RCV000164587.1, RCV000217263.1,