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rs876660755

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs876660755(-;-)
Make rs876660755(-;A)
ReferenceGRCh38.p2 38.2/147
Chromosome13
Position32338802
GeneBRCA2
is asnp
is mentioned by
dbSNPrs876660755
ebirs876660755
HLIrs876660755
Exacrs876660755
Varsomers876660755
Maprs876660755
PheGenIrs876660755
hapmaprs876660755
1000 genomesrs876660755
hgdprs876660755
ensemblrs876660755
gopubmedrs876660755
geneviewrs876660755
scholarrs876660755
googlers876660755
pharmgkbrs876660755
gwascentralrs876660755
openSNPrs876660755
23andMers876660755
23andMe allrs876660755
SNP Nexus

SNPshotrs876660755
SNPdbers876660755
MSV3drs876660755
GWAS Ctlgrs876660755
Max Magnitude0
ClinVar
Risk rs876660755(;)
Alt rs876660755(;)
Reference rs876660755(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.32912939delA
CLNSRC
CLNACC RCV000218196.1,