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rs876658643

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs876658643(-;-)
Make rs876658643(-;T)
ReferenceGRCh38.p2 38.2/147
Chromosome13
Position32394710
GeneBRCA2
is asnp
is mentioned by
dbSNPrs876658643
ebirs876658643
HLIrs876658643
Exacrs876658643
Varsomers876658643
Maprs876658643
PheGenIrs876658643
hapmaprs876658643
1000 genomesrs876658643
hgdprs876658643
ensemblrs876658643
gopubmedrs876658643
geneviewrs876658643
scholarrs876658643
googlers876658643
pharmgkbrs876658643
gwascentralrs876658643
openSNPrs876658643
23andMers876658643
23andMe allrs876658643
SNP Nexus

SNPshotrs876658643
SNPdbers876658643
MSV3drs876658643
GWAS Ctlgrs876658643
Max Magnitude0
ClinVar
Risk rs876658643(;)
Alt rs876658643(;)
Reference rs876658643(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.32968847delT
CLNSRC
CLNACC RCV000222200.1,