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rs876659359

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs876659359(A;A)
Make rs876659359(A;T)
ReferenceGRCh38.p2 38.2/147
Chromosome13
Position32332366
GeneBRCA2
is asnp
is mentioned by
dbSNPrs876659359
ebirs876659359
HLIrs876659359
Exacrs876659359
Varsomers876659359
Maprs876659359
PheGenIrs876659359
hapmaprs876659359
1000 genomesrs876659359
hgdprs876659359
ensemblrs876659359
gopubmedrs876659359
geneviewrs876659359
scholarrs876659359
googlers876659359
pharmgkbrs876659359
gwascentralrs876659359
openSNPrs876659359
23andMers876659359
23andMe allrs876659359
SNP Nexus

SNPshotrs876659359
SNPdbers876659359
MSV3drs876659359
GWAS Ctlgrs876659359
Max Magnitude0
ClinVar
Risk rs876659359(A;A)
Alt rs876659359(A;A)
Reference rs876659359(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.32906503T>A
CLNSRC
CLNACC RCV000219527.1,