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rs876658470

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs876658470(-;-)
Make rs876658470(-;G)
ReferenceGRCh38.p2 38.2/147
Chromosome13
Position32356594
GeneBRCA2
is asnp
is mentioned by
dbSNPrs876658470
ebirs876658470
HLIrs876658470
Exacrs876658470
Varsomers876658470
Maprs876658470
PheGenIrs876658470
hapmaprs876658470
1000 genomesrs876658470
hgdprs876658470
ensemblrs876658470
gopubmedrs876658470
geneviewrs876658470
scholarrs876658470
googlers876658470
pharmgkbrs876658470
gwascentralrs876658470
openSNPrs876658470
23andMers876658470
23andMe allrs876658470
SNP Nexus

SNPshotrs876658470
SNPdbers876658470
MSV3drs876658470
GWAS Ctlgrs876658470
Max Magnitude0
ClinVar
Risk rs876658470(;)
Alt rs876658470(;)
Reference rs876658470(G;G)
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.32930731delG
CLNSRC
CLNACC RCV000223321.1,