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rs786204931

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs786204931(C;T)
Make rs786204931(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome10
Position87933126
GenePTEN
is asnp
is mentioned by
dbSNPrs786204931
ebirs786204931
HLIrs786204931
Exacrs786204931
Varsomers786204931
Maprs786204931
PheGenIrs786204931
hapmaprs786204931
1000 genomesrs786204931
hgdprs786204931
ensemblrs786204931
gopubmedrs786204931
geneviewrs786204931
scholarrs786204931
googlers786204931
pharmgkbrs786204931
gwascentralrs786204931
openSNPrs786204931
23andMers786204931
23andMe allrs786204931
SNP Nexus

SNPshotrs786204931
SNPdbers786204931
MSV3drs786204931
GWAS Ctlgrs786204931
Max Magnitude0
ClinVar
Risk rs786204931(T;T)
Alt rs786204931(T;T)
Reference rs786204931(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene PTEN
CLNDBN not provided
Reversed 0
HGVS NC_000010.10:g.89692883C>T
CLNSRC
CLNACC RCV000169876.1,