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

rs786204926

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs786204926(A;G)
Make rs786204926(G;G)
ReferenceGRCh38.p2 38.2/146
Chromosome10
Position87933011
GenePTEN
is asnp
is mentioned by
dbSNPrs786204926
ebirs786204926
HLIrs786204926
Exacrs786204926
Varsomers786204926
Maprs786204926
PheGenIrs786204926
hapmaprs786204926
1000 genomesrs786204926
hgdprs786204926
ensemblrs786204926
gopubmedrs786204926
geneviewrs786204926
scholarrs786204926
googlers786204926
pharmgkbrs786204926
gwascentralrs786204926
openSNPrs786204926
23andMers786204926
23andMe allrs786204926
SNP Nexus

SNPshotrs786204926
SNPdbers786204926
MSV3drs786204926
GWAS Ctlgrs786204926
Max Magnitude0
ClinVar
Risk rs786204926(G;G)
Alt rs786204926(G;G)
Reference rs786204926(A;A)
Significance Pathogenic
Disease not provided
Variation info
Gene PTEN
CLNDBN not provided
Reversed 0
HGVS NC_000010.10:g.89692768A>G
CLNSRC
CLNACC RCV000169871.1,