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rs876658929

From SNPedia

Orientationplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs876658929(-;-)
Make rs876658929(-;T)
Make rs876658929(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome13
Position32336966
GeneBRCA2
is asnp
is mentioned by
dbSNPrs876658929
ebirs876658929
HLIrs876658929
Exacrs876658929
Varsomers876658929
Maprs876658929
PheGenIrs876658929
hapmaprs876658929
1000 genomesrs876658929
hgdprs876658929
ensemblrs876658929
gopubmedrs876658929
geneviewrs876658929
scholarrs876658929
googlers876658929
pharmgkbrs876658929
gwascentralrs876658929
openSNPrs876658929
23andMers876658929
23andMe allrs876658929
SNP Nexus

SNPshotrs876658929
SNPdbers876658929
MSV3drs876658929
GWAS Ctlgrs876658929
Max Magnitude0
ClinVar
Risk rs876658929(T;T)
Alt rs876658929(T;T)
Reference rs876658929(;)
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.32911103dupT
CLNSRC
CLNACC RCV000218545.1,