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rs876659767

From SNPedia

Orientationplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs876659767(-;-)
Make rs876659767(-;A)
Make rs876659767(A;A)
ReferenceGRCh38.p2 38.2/147
Chromosome13
Position32337071
GeneBRCA2
is asnp
is mentioned by
dbSNPrs876659767
ebirs876659767
HLIrs876659767
Exacrs876659767
Varsomers876659767
Maprs876659767
PheGenIrs876659767
hapmaprs876659767
1000 genomesrs876659767
hgdprs876659767
ensemblrs876659767
gopubmedrs876659767
geneviewrs876659767
scholarrs876659767
googlers876659767
pharmgkbrs876659767
gwascentralrs876659767
openSNPrs876659767
23andMers876659767
23andMe allrs876659767
SNP Nexus

SNPshotrs876659767
SNPdbers876659767
MSV3drs876659767
GWAS Ctlgrs876659767
Max Magnitude0
ClinVar
Risk rs876659767(A;A)
Alt rs876659767(A;A)
Reference rs876659767(;)
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.32911208dupA
CLNSRC
CLNACC RCV000221474.1,