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

rs876660599

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs876660599(-;-)
Make rs876660599(-;T)
ReferenceGRCh38.p2 38.2/147
Chromosome13
Position32380122
GeneBRCA2
is asnp
is mentioned by
dbSNPrs876660599
ebirs876660599
HLIrs876660599
Exacrs876660599
Varsomers876660599
Maprs876660599
PheGenIrs876660599
hapmaprs876660599
1000 genomesrs876660599
hgdprs876660599
ensemblrs876660599
gopubmedrs876660599
geneviewrs876660599
scholarrs876660599
googlers876660599
pharmgkbrs876660599
gwascentralrs876660599
openSNPrs876660599
23andMers876660599
23andMe allrs876660599
SNP Nexus

SNPshotrs876660599
SNPdbers876660599
MSV3drs876660599
GWAS Ctlgrs876660599
Max Magnitude0
ClinVar
Risk rs876660599(;)
Alt rs876660599(;)
Reference rs876660599(T;T)
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.32954259delT
CLNSRC
CLNACC RCV000213244.1,