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rs876659236

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs876659236(-;-)
Make rs876659236(-;T)
ReferenceGRCh38.p2 38.2/147
Chromosome13
Position32339663
GeneBRCA2
is asnp
is mentioned by
dbSNPrs876659236
ebirs876659236
HLIrs876659236
Exacrs876659236
Varsomers876659236
Maprs876659236
PheGenIrs876659236
hapmaprs876659236
1000 genomesrs876659236
hgdprs876659236
ensemblrs876659236
gopubmedrs876659236
geneviewrs876659236
scholarrs876659236
googlers876659236
pharmgkbrs876659236
gwascentralrs876659236
openSNPrs876659236
23andMers876659236
23andMe allrs876659236
SNP Nexus

SNPshotrs876659236
SNPdbers876659236
MSV3drs876659236
GWAS Ctlgrs876659236
Max Magnitude0
ClinVar
Risk rs876659236(;)
Alt rs876659236(;)
Reference rs876659236(T;T)
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.32913800delT
CLNSRC
CLNACC RCV000213627.1,