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rs876660504

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs876660504(-;-)
Make rs876660504(-;C)
ReferenceGRCh38.p2 38.2/147
Chromosome13
Position32319185
GeneBRCA2
is asnp
is mentioned by
dbSNPrs876660504
ebirs876660504
HLIrs876660504
Exacrs876660504
Varsomers876660504
Maprs876660504
PheGenIrs876660504
hapmaprs876660504
1000 genomesrs876660504
hgdprs876660504
ensemblrs876660504
gopubmedrs876660504
geneviewrs876660504
scholarrs876660504
googlers876660504
pharmgkbrs876660504
gwascentralrs876660504
openSNPrs876660504
23andMers876660504
23andMe allrs876660504
SNP Nexus

SNPshotrs876660504
SNPdbers876660504
MSV3drs876660504
GWAS Ctlgrs876660504
Max Magnitude0
ClinVar
Risk rs876660504(;)
Alt rs876660504(;)
Reference rs876660504(C;C)
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.32893322delC
CLNSRC
CLNACC RCV000213638.1,