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

rs876660524

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs876660524(-;-)
Make rs876660524(-;G)
ReferenceGRCh38.p2 38.2/147
Chromosome13
Position32339431
GeneBRCA2
is asnp
is mentioned by
dbSNPrs876660524
ebirs876660524
HLIrs876660524
Exacrs876660524
Varsomers876660524
Maprs876660524
PheGenIrs876660524
hapmaprs876660524
1000 genomesrs876660524
hgdprs876660524
ensemblrs876660524
gopubmedrs876660524
geneviewrs876660524
scholarrs876660524
googlers876660524
pharmgkbrs876660524
gwascentralrs876660524
openSNPrs876660524
23andMers876660524
23andMe allrs876660524
SNP Nexus

SNPshotrs876660524
SNPdbers876660524
MSV3drs876660524
GWAS Ctlgrs876660524
Max Magnitude0
ClinVar
Risk rs876660524(;)
Alt rs876660524(;)
Reference rs876660524(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.32913568delG
CLNSRC
CLNACC RCV000220340.1,