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rs876659318

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs876659318(-;-)
Make rs876659318(-;C)
ReferenceGRCh38.p2 38.2/147
Chromosome13
Position32336611
GeneBRCA2
is asnp
is mentioned by
dbSNPrs876659318
ebirs876659318
HLIrs876659318
Exacrs876659318
Varsomers876659318
Maprs876659318
PheGenIrs876659318
hapmaprs876659318
1000 genomesrs876659318
hgdprs876659318
ensemblrs876659318
gopubmedrs876659318
geneviewrs876659318
scholarrs876659318
googlers876659318
pharmgkbrs876659318
gwascentralrs876659318
openSNPrs876659318
23andMers876659318
23andMe allrs876659318
SNP Nexus

SNPshotrs876659318
SNPdbers876659318
MSV3drs876659318
GWAS Ctlgrs876659318
Max Magnitude0
ClinVar
Risk rs876659318(;)
Alt rs876659318(;)
Reference rs876659318(C;C)
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.32910748delC
CLNSRC
CLNACC RCV000220476.1,