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rs876658648

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs876658648(G;T)
Make rs876658648(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome13
Position32336996
GeneBRCA2
is asnp
is mentioned by
dbSNPrs876658648
ebirs876658648
HLIrs876658648
Exacrs876658648
Varsomers876658648
Maprs876658648
PheGenIrs876658648
hapmaprs876658648
1000 genomesrs876658648
hgdprs876658648
ensemblrs876658648
gopubmedrs876658648
geneviewrs876658648
scholarrs876658648
googlers876658648
pharmgkbrs876658648
gwascentralrs876658648
openSNPrs876658648
23andMers876658648
23andMe allrs876658648
SNP Nexus

SNPshotrs876658648
SNPdbers876658648
MSV3drs876658648
GWAS Ctlgrs876658648
Max Magnitude0
ClinVar
Risk rs876658648(T;T)
Alt rs876658648(T;T)
Reference rs876658648(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.32911133G>T
CLNSRC
CLNACC RCV000213781.1,