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rs876658294

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs876658294(-;-)
Make rs876658294(-;C)
ReferenceGRCh38.p2 38.2/147
Chromosome13
Position32340951
GeneBRCA2
is asnp
is mentioned by
dbSNPrs876658294
ebirs876658294
HLIrs876658294
Exacrs876658294
Varsomers876658294
Maprs876658294
PheGenIrs876658294
hapmaprs876658294
1000 genomesrs876658294
hgdprs876658294
ensemblrs876658294
gopubmedrs876658294
geneviewrs876658294
scholarrs876658294
googlers876658294
pharmgkbrs876658294
gwascentralrs876658294
openSNPrs876658294
23andMers876658294
23andMe allrs876658294
SNP Nexus

SNPshotrs876658294
SNPdbers876658294
MSV3drs876658294
GWAS Ctlgrs876658294
Max Magnitude0
ClinVar
Risk rs876658294(;)
Alt rs876658294(;)
Reference rs876658294(C;C)
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.32915088delC
CLNSRC
CLNACC RCV000217392.1,