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rs876659278

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs876659278(-;-)
Make rs876659278(-;G)
ReferenceGRCh38.p2 38.2/147
Chromosome13
Position32333167
GeneBRCA2
is asnp
is mentioned by
dbSNPrs876659278
ebirs876659278
HLIrs876659278
Exacrs876659278
Varsomers876659278
Maprs876659278
PheGenIrs876659278
hapmaprs876659278
1000 genomesrs876659278
hgdprs876659278
ensemblrs876659278
gopubmedrs876659278
geneviewrs876659278
scholarrs876659278
googlers876659278
pharmgkbrs876659278
gwascentralrs876659278
openSNPrs876659278
23andMers876659278
23andMe allrs876659278
SNP Nexus

SNPshotrs876659278
SNPdbers876659278
MSV3drs876659278
GWAS Ctlgrs876659278
Max Magnitude0
ClinVar
Risk rs876659278(;)
Alt rs876659278(;)
Reference rs876659278(G;G)
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.32907304delG
CLNSRC
CLNACC RCV000213086.1,