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rs786204914

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs786204914(C;C)
Make rs786204914(C;G)
ReferenceGRCh38.p2 38.2/146
Chromosome10
Position87894024
GenePTEN
is asnp
is mentioned by
dbSNPrs786204914
ebirs786204914
HLIrs786204914
Exacrs786204914
Varsomers786204914
Maprs786204914
PheGenIrs786204914
hapmaprs786204914
1000 genomesrs786204914
hgdprs786204914
ensemblrs786204914
gopubmedrs786204914
geneviewrs786204914
scholarrs786204914
googlers786204914
pharmgkbrs786204914
gwascentralrs786204914
openSNPrs786204914
23andMers786204914
23andMe allrs786204914
SNP Nexus

SNPshotrs786204914
SNPdbers786204914
MSV3drs786204914
GWAS Ctlgrs786204914
Max Magnitude0
ClinVar
Risk rs786204914(C;C)
Alt rs786204914(C;C)
Reference rs786204914(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene PTEN
CLNDBN not provided
Reversed 0
HGVS NC_000010.10:g.89653781G>C
CLNSRC
CLNACC RCV000169855.1,