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rs876659482

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs876659482(-;-)
Make rs876659482(-;G)
ReferenceGRCh38.p2 38.2/147
Chromosome13
Position32339712
GeneBRCA2
is asnp
is mentioned by
dbSNPrs876659482
ebirs876659482
HLIrs876659482
Exacrs876659482
Varsomers876659482
Maprs876659482
PheGenIrs876659482
hapmaprs876659482
1000 genomesrs876659482
hgdprs876659482
ensemblrs876659482
gopubmedrs876659482
geneviewrs876659482
scholarrs876659482
googlers876659482
pharmgkbrs876659482
gwascentralrs876659482
openSNPrs876659482
23andMers876659482
23andMe allrs876659482
SNP Nexus

SNPshotrs876659482
SNPdbers876659482
MSV3drs876659482
GWAS Ctlgrs876659482
Max Magnitude0
ClinVar
Risk rs876659482(;)
Alt rs876659482(;)
Reference rs876659482(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.32913849delG
CLNSRC
CLNACC RCV000213290.1,