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rs876658329

From SNPedia

Orientationplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs876658329(-;-)
Make rs876658329(-;AA)
Make rs876658329(AA;AA)
ReferenceGRCh38.p2 38.2/147
Chromosome13
Position32338447
GeneBRCA2
is asnp
is mentioned by
dbSNPrs876658329
ebirs876658329
HLIrs876658329
Exacrs876658329
Varsomers876658329
Maprs876658329
PheGenIrs876658329
hapmaprs876658329
1000 genomesrs876658329
hgdprs876658329
ensemblrs876658329
gopubmedrs876658329
geneviewrs876658329
scholarrs876658329
googlers876658329
pharmgkbrs876658329
gwascentralrs876658329
openSNPrs876658329
23andMers876658329
23andMe allrs876658329
SNP Nexus

SNPshotrs876658329
SNPdbers876658329
MSV3drs876658329
GWAS Ctlgrs876658329
Max Magnitude0
ClinVar
Risk rs876658329(AA;AA)
Alt rs876658329(AA;AA)
Reference rs876658329(;)
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.32912584_32912585insAA
CLNSRC
CLNACC RCV000216793.1,