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rs876660026

From SNPedia

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Geno Mag Summary
(AA;AA) 0 common in clinvar
Make rs876660026(-;-)
Make rs876660026(-;AA)
ReferenceGRCh38.p2 38.2/147
Chromosome13
Position32338815
GeneBRCA2
is asnp
is mentioned by
dbSNPrs876660026
ebirs876660026
HLIrs876660026
Exacrs876660026
Varsomers876660026
Maprs876660026
PheGenIrs876660026
hapmaprs876660026
1000 genomesrs876660026
hgdprs876660026
ensemblrs876660026
gopubmedrs876660026
geneviewrs876660026
scholarrs876660026
googlers876660026
pharmgkbrs876660026
gwascentralrs876660026
openSNPrs876660026
23andMers876660026
23andMe allrs876660026
SNP Nexus

SNPshotrs876660026
SNPdbers876660026
MSV3drs876660026
GWAS Ctlgrs876660026
Max Magnitude0
ClinVar
Risk rs876660026(;)
Alt rs876660026(;)
Reference rs876660026(AA;AA)
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.32912952_32912953delAA
CLNSRC
CLNACC RCV000214586.1,