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rs876658927

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs876658927(-;-)
Make rs876658927(-;A)
ReferenceGRCh38.p2 38.2/147
Chromosome13
Position32330970
GeneBRCA2
is asnp
is mentioned by
dbSNPrs876658927
ebirs876658927
HLIrs876658927
Exacrs876658927
Varsomers876658927
Maprs876658927
PheGenIrs876658927
hapmaprs876658927
1000 genomesrs876658927
hgdprs876658927
ensemblrs876658927
gopubmedrs876658927
geneviewrs876658927
scholarrs876658927
googlers876658927
pharmgkbrs876658927
gwascentralrs876658927
openSNPrs876658927
23andMers876658927
23andMe allrs876658927
SNP Nexus

SNPshotrs876658927
SNPdbers876658927
MSV3drs876658927
GWAS Ctlgrs876658927
Max Magnitude0
ClinVar
Risk rs876658927(;)
Alt rs876658927(;)
Reference rs876658927(A;A)
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.32905107delA
CLNSRC
CLNACC RCV000213136.1,