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rs876660510

From SNPedia

Orientationplus
Geno Mag Summary
(CT;CT) 0 common in clinvar
Make rs876660510(-;-)
Make rs876660510(-;CT)
ReferenceGRCh38.p2 38.2/147
Chromosome13
Position32338738
GeneBRCA2
is asnp
is mentioned by
dbSNPrs876660510
ebirs876660510
HLIrs876660510
Exacrs876660510
Varsomers876660510
Maprs876660510
PheGenIrs876660510
hapmaprs876660510
1000 genomesrs876660510
hgdprs876660510
ensemblrs876660510
gopubmedrs876660510
geneviewrs876660510
scholarrs876660510
googlers876660510
pharmgkbrs876660510
gwascentralrs876660510
openSNPrs876660510
23andMers876660510
23andMe allrs876660510
SNP Nexus

SNPshotrs876660510
SNPdbers876660510
MSV3drs876660510
GWAS Ctlgrs876660510
Max Magnitude0
ClinVar
Risk rs876660510(;)
Alt rs876660510(;)
Reference rs876660510(CT;CT)
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.32912875_32912876delCT
CLNSRC
CLNACC RCV000223548.1,