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rs876659977

From SNPedia

Orientationplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs876659977(-;-)
Make rs876659977(-;G)
Make rs876659977(G;G)
ReferenceGRCh38.p2 38.2/147
Chromosome13
Position32338532
GeneBRCA2
is asnp
is mentioned by
dbSNPrs876659977
ebirs876659977
HLIrs876659977
Exacrs876659977
Varsomers876659977
Maprs876659977
PheGenIrs876659977
hapmaprs876659977
1000 genomesrs876659977
hgdprs876659977
ensemblrs876659977
gopubmedrs876659977
geneviewrs876659977
scholarrs876659977
googlers876659977
pharmgkbrs876659977
gwascentralrs876659977
openSNPrs876659977
23andMers876659977
23andMe allrs876659977
SNP Nexus

SNPshotrs876659977
SNPdbers876659977
MSV3drs876659977
GWAS Ctlgrs876659977
Max Magnitude0
ClinVar
Risk rs876659977(G;G)
Alt rs876659977(G;G)
Reference rs876659977(;)
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.32912669dupG
CLNSRC
CLNACC RCV000214720.1,