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rs876658427

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs876658427(-;-)
Make rs876658427(-;A)
ReferenceGRCh38.p2 38.2/147
Chromosome13
Position32337751
GeneBRCA2
is asnp
is mentioned by
dbSNPrs876658427
ebirs876658427
HLIrs876658427
Exacrs876658427
Varsomers876658427
Maprs876658427
PheGenIrs876658427
hapmaprs876658427
1000 genomesrs876658427
hgdprs876658427
ensemblrs876658427
gopubmedrs876658427
geneviewrs876658427
scholarrs876658427
googlers876658427
pharmgkbrs876658427
gwascentralrs876658427
openSNPrs876658427
23andMers876658427
23andMe allrs876658427
SNP Nexus

SNPshotrs876658427
SNPdbers876658427
MSV3drs876658427
GWAS Ctlgrs876658427
Max Magnitude0
ClinVar
Risk rs876658427(;)
Alt rs876658427(;)
Reference rs876658427(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.32911888delA
CLNSRC
CLNACC RCV000216535.1,