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rs876660532

From SNPedia

Orientationplus
Geno Mag Summary
(AA;AA) 0 common in clinvar
Make rs876660532(AA;G)
Make rs876660532(G;G)
ReferenceGRCh38.p2 38.2/147
Chromosome13
Position32379889
GeneBRCA2
is asnp
is mentioned by
dbSNPrs876660532
ebirs876660532
HLIrs876660532
Exacrs876660532
Varsomers876660532
Maprs876660532
PheGenIrs876660532
hapmaprs876660532
1000 genomesrs876660532
hgdprs876660532
ensemblrs876660532
gopubmedrs876660532
geneviewrs876660532
scholarrs876660532
googlers876660532
pharmgkbrs876660532
gwascentralrs876660532
openSNPrs876660532
23andMers876660532
23andMe allrs876660532
SNP Nexus

SNPshotrs876660532
SNPdbers876660532
MSV3drs876660532
GWAS Ctlgrs876660532
Max Magnitude0
ClinVar
Risk rs876660532(G;G)
Alt rs876660532(G;G)
Reference rs876660532(AA;AA)
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.32954026_32954027delAAinsG
CLNSRC
CLNACC RCV000222945.1,