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rs876658789

From SNPedia

Orientationplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs876658789(-;-)
Make rs876658789(-;T)
Make rs876658789(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome13
Position32346879
GeneBRCA2
is asnp
is mentioned by
dbSNPrs876658789
ebirs876658789
HLIrs876658789
Exacrs876658789
Varsomers876658789
Maprs876658789
PheGenIrs876658789
hapmaprs876658789
1000 genomesrs876658789
hgdprs876658789
ensemblrs876658789
gopubmedrs876658789
geneviewrs876658789
scholarrs876658789
googlers876658789
pharmgkbrs876658789
gwascentralrs876658789
openSNPrs876658789
23andMers876658789
23andMe allrs876658789
SNP Nexus

SNPshotrs876658789
SNPdbers876658789
MSV3drs876658789
GWAS Ctlgrs876658789
Max Magnitude0
ClinVar
Risk rs876658789(T;T)
Alt rs876658789(T;T)
Reference rs876658789(;)
Significance Pathogenic
Disease Tumor susceptibility linked to germline BAP1 mutations
Variation info
Gene BRCA2
CLNDBN Tumor susceptibility linked to germline BAP1 mutations
Reversed 0
HGVS NC_000013.10:g.32921016dupT
CLNSRC
CLNACC RCV000222923.1,