Have questions? Visit https://www.reddit.com/r/SNPedia

rs876658861

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs876658861(-;-)
Make rs876658861(-;C)
ReferenceGRCh38.p2 38.2/147
Chromosome13
Position32332312
GeneBRCA2
is asnp
is mentioned by
dbSNPrs876658861
ebirs876658861
HLIrs876658861
Exacrs876658861
Varsomers876658861
Maprs876658861
PheGenIrs876658861
hapmaprs876658861
1000 genomesrs876658861
hgdprs876658861
ensemblrs876658861
gopubmedrs876658861
geneviewrs876658861
scholarrs876658861
googlers876658861
pharmgkbrs876658861
gwascentralrs876658861
openSNPrs876658861
23andMers876658861
23andMe allrs876658861
SNP Nexus

SNPshotrs876658861
SNPdbers876658861
MSV3drs876658861
GWAS Ctlgrs876658861
Max Magnitude0
ClinVar
Risk rs876658861(;)
Alt rs876658861(;)
Reference rs876658861(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.32906449delC
CLNSRC
CLNACC RCV000216017.1,