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rs876659261

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs876659261(-;-)
Make rs876659261(-;A)
ReferenceGRCh38.p2 38.2/147
Chromosome13
Position32329479
GeneBRCA2
is asnp
is mentioned by
dbSNPrs876659261
ebirs876659261
HLIrs876659261
Exacrs876659261
Varsomers876659261
Maprs876659261
PheGenIrs876659261
hapmaprs876659261
1000 genomesrs876659261
hgdprs876659261
ensemblrs876659261
gopubmedrs876659261
geneviewrs876659261
scholarrs876659261
googlers876659261
pharmgkbrs876659261
gwascentralrs876659261
openSNPrs876659261
23andMers876659261
23andMe allrs876659261
SNP Nexus

SNPshotrs876659261
SNPdbers876659261
MSV3drs876659261
GWAS Ctlgrs876659261
Max Magnitude0
ClinVar
Risk rs876659261(;)
Alt rs876659261(;)
Reference rs876659261(A;A)
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.32903616delA
CLNSRC
CLNACC RCV000214075.1,