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rs876658577

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs876658577(A;A)
Make rs876658577(A;T)
ReferenceGRCh38.p2 38.2/147
Chromosome13
Position32333389
GeneBRCA2
is asnp
is mentioned by
dbSNPrs876658577
ebirs876658577
HLIrs876658577
Exacrs876658577
Varsomers876658577
Maprs876658577
PheGenIrs876658577
hapmaprs876658577
1000 genomesrs876658577
hgdprs876658577
ensemblrs876658577
gopubmedrs876658577
geneviewrs876658577
scholarrs876658577
googlers876658577
pharmgkbrs876658577
gwascentralrs876658577
openSNPrs876658577
23andMers876658577
23andMe allrs876658577
SNP Nexus

SNPshotrs876658577
SNPdbers876658577
MSV3drs876658577
GWAS Ctlgrs876658577
Max Magnitude0
ClinVar
Risk rs876658577(A;A)
Alt rs876658577(A;A)
Reference rs876658577(T;T)
Significance Probable-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.32907526T>A
CLNSRC
CLNACC RCV000214167.1,