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rs876660512

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs876660512(A;A)
Make rs876660512(A;T)
ReferenceGRCh38.p2 38.2/147
Chromosome13
Position32336506
GeneBRCA2
is asnp
is mentioned by
dbSNPrs876660512
ebirs876660512
HLIrs876660512
Exacrs876660512
Varsomers876660512
Maprs876660512
PheGenIrs876660512
hapmaprs876660512
1000 genomesrs876660512
hgdprs876660512
ensemblrs876660512
gopubmedrs876660512
geneviewrs876660512
scholarrs876660512
googlers876660512
pharmgkbrs876660512
gwascentralrs876660512
openSNPrs876660512
23andMers876660512
23andMe allrs876660512
SNP Nexus

SNPshotrs876660512
SNPdbers876660512
MSV3drs876660512
GWAS Ctlgrs876660512
Max Magnitude0
ClinVar
Risk rs876660512(A;A)
Alt rs876660512(A;A)
Reference rs876660512(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.32910643T>A
CLNSRC
CLNACC RCV000213890.1,