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rs786204862

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs786204862(A;A)
Make rs786204862(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome10
Position87952117
GenePTEN
is asnp
is mentioned by
dbSNPrs786204862
ebirs786204862
HLIrs786204862
Exacrs786204862
Varsomers786204862
Maprs786204862
PheGenIrs786204862
hapmaprs786204862
1000 genomesrs786204862
hgdprs786204862
ensemblrs786204862
gopubmedrs786204862
geneviewrs786204862
scholarrs786204862
googlers786204862
pharmgkbrs786204862
gwascentralrs786204862
openSNPrs786204862
23andMers786204862
23andMe allrs786204862
SNP Nexus

SNPshotrs786204862
SNPdbers786204862
MSV3drs786204862
GWAS Ctlgrs786204862
Max Magnitude0
ClinVar
Risk rs786204862(A;A)
Alt rs786204862(A;A)
Reference rs786204862(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene PTEN
CLNDBN not provided
Reversed 0
HGVS NC_000010.10:g.89711874G>A
CLNSRC
CLNACC RCV000169802.2,