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rs876659258

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs876659258(A;A)
Make rs876659258(A;C)
ReferenceGRCh38.p2 38.2/147
Chromosome13
Position32337760
GeneBRCA2
is asnp
is mentioned by
dbSNPrs876659258
ebirs876659258
HLIrs876659258
Exacrs876659258
Varsomers876659258
Maprs876659258
PheGenIrs876659258
hapmaprs876659258
1000 genomesrs876659258
hgdprs876659258
ensemblrs876659258
gopubmedrs876659258
geneviewrs876659258
scholarrs876659258
googlers876659258
pharmgkbrs876659258
gwascentralrs876659258
openSNPrs876659258
23andMers876659258
23andMe allrs876659258
SNP Nexus

SNPshotrs876659258
SNPdbers876659258
MSV3drs876659258
GWAS Ctlgrs876659258
Max Magnitude0
ClinVar
Risk rs876659258(A;A)
Alt rs876659258(A;A)
Reference rs876659258(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.32911897C>A
CLNSRC
CLNACC RCV000216708.1,