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rs876660636

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs876660636(-;-)
Make rs876660636(-;A)
ReferenceGRCh38.p2 38.2/147
Chromosome13
Position32339985
GeneBRCA2
is asnp
is mentioned by
dbSNPrs876660636
ebirs876660636
HLIrs876660636
Exacrs876660636
Varsomers876660636
Maprs876660636
PheGenIrs876660636
hapmaprs876660636
1000 genomesrs876660636
hgdprs876660636
ensemblrs876660636
gopubmedrs876660636
geneviewrs876660636
scholarrs876660636
googlers876660636
pharmgkbrs876660636
gwascentralrs876660636
openSNPrs876660636
23andMers876660636
23andMe allrs876660636
SNP Nexus

SNPshotrs876660636
SNPdbers876660636
MSV3drs876660636
GWAS Ctlgrs876660636
Max Magnitude0
ClinVar
Risk rs876660636(;)
Alt rs876660636(;)
Reference rs876660636(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.32914122delA
CLNSRC
CLNACC RCV000214774.1,