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rs876658660

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs876658660(-;-)
Make rs876658660(-;C)
ReferenceGRCh38.p2 38.2/147
Chromosome13
Position32336298
GeneBRCA2
is asnp
is mentioned by
dbSNPrs876658660
ebirs876658660
HLIrs876658660
Exacrs876658660
Varsomers876658660
Maprs876658660
PheGenIrs876658660
hapmaprs876658660
1000 genomesrs876658660
hgdprs876658660
ensemblrs876658660
gopubmedrs876658660
geneviewrs876658660
scholarrs876658660
googlers876658660
pharmgkbrs876658660
gwascentralrs876658660
openSNPrs876658660
23andMers876658660
23andMe allrs876658660
SNP Nexus

SNPshotrs876658660
SNPdbers876658660
MSV3drs876658660
GWAS Ctlgrs876658660
Max Magnitude0
ClinVar
Risk rs876658660(;)
Alt rs876658660(;)
Reference rs876658660(C;C)
Significance Pathogenic
Disease Tumor susceptibility linked to germline BAP1 mutations Breast-ovarian cancer
Variation info
Gene BRCA2
CLNDBN Tumor susceptibility linked to germline BAP1 mutations Breast-ovarian cancer, familial 2
Reversed 0
HGVS NC_000013.10:g.32910435delC
CLNSRC
CLNACC RCV000214005.1, RCV000238927.1,