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rs876659443

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs876659443(A;G)
Make rs876659443(G;G)
ReferenceGRCh38.p2 38.2/147
Chromosome10
Position87894048
GenePTEN
is asnp
is mentioned by
dbSNPrs876659443
ebirs876659443
HLIrs876659443
Exacrs876659443
Varsomers876659443
Maprs876659443
PheGenIrs876659443
hapmaprs876659443
1000 genomesrs876659443
hgdprs876659443
ensemblrs876659443
gopubmedrs876659443
geneviewrs876659443
scholarrs876659443
googlers876659443
pharmgkbrs876659443
gwascentralrs876659443
openSNPrs876659443
23andMers876659443
23andMe allrs876659443
SNP Nexus

SNPshotrs876659443
SNPdbers876659443
MSV3drs876659443
GWAS Ctlgrs876659443
Max Magnitude0
ClinVar
Risk rs876659443(G;G)
Alt rs876659443(G;G)
Reference rs876659443(A;A)
Significance Probable-Pathogenic
Disease Tumor susceptibility linked to germline BAP1 mutations
Variation info
Gene PTEN
CLNDBN Tumor susceptibility linked to germline BAP1 mutations
Reversed 0
HGVS NC_000010.10:g.89653805A>G
CLNSRC
CLNACC RCV000218360.1,