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rs876659368

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs876659368(A;A)
Make rs876659368(A;T)
ReferenceGRCh38.p2 38.2/147
Chromosome13
Position32340706
GeneBRCA2
is asnp
is mentioned by
dbSNPrs876659368
ebirs876659368
HLIrs876659368
Exacrs876659368
Varsomers876659368
Maprs876659368
PheGenIrs876659368
hapmaprs876659368
1000 genomesrs876659368
hgdprs876659368
ensemblrs876659368
gopubmedrs876659368
geneviewrs876659368
scholarrs876659368
googlers876659368
pharmgkbrs876659368
gwascentralrs876659368
openSNPrs876659368
23andMers876659368
23andMe allrs876659368
SNP Nexus

SNPshotrs876659368
SNPdbers876659368
MSV3drs876659368
GWAS Ctlgrs876659368
Max Magnitude0
ClinVar
Risk rs876659368(A;A)
Alt rs876659368(A;A)
Reference rs876659368(T;T)
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.32914843T>A
CLNSRC
CLNACC RCV000221121.1,