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rs876659617

From SNPedia

Orientationplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs876659617(-;-)
Make rs876659617(-;A)
Make rs876659617(A;A)
ReferenceGRCh38.p2 38.2/147
Chromosome13
Position32340687
GeneBRCA2
is asnp
is mentioned by
dbSNPrs876659617
ebirs876659617
HLIrs876659617
Exacrs876659617
Varsomers876659617
Maprs876659617
PheGenIrs876659617
hapmaprs876659617
1000 genomesrs876659617
hgdprs876659617
ensemblrs876659617
gopubmedrs876659617
geneviewrs876659617
scholarrs876659617
googlers876659617
pharmgkbrs876659617
gwascentralrs876659617
openSNPrs876659617
23andMers876659617
23andMe allrs876659617
SNP Nexus

SNPshotrs876659617
SNPdbers876659617
MSV3drs876659617
GWAS Ctlgrs876659617
Max Magnitude0
ClinVar
Risk rs876659617(A;A)
Alt rs876659617(A;A)
Reference rs876659617(;)
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.32914824dupA
CLNSRC
CLNACC RCV000220761.1,