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rs876658928

From SNPedia

Orientationplus
Geno Mag Summary
(TG;TG) 0 common in clinvar
Make rs876658928(-;-)
Make rs876658928(-;GT)
Make rs876658928(GT;GT)
ReferenceGRCh38.p2 38.2/147
Chromosome13
Position32336978
GeneBRCA2
is asnp
is mentioned by
dbSNPrs876658928
ebirs876658928
HLIrs876658928
Exacrs876658928
Varsomers876658928
Maprs876658928
PheGenIrs876658928
hapmaprs876658928
1000 genomesrs876658928
hgdprs876658928
ensemblrs876658928
gopubmedrs876658928
geneviewrs876658928
scholarrs876658928
googlers876658928
pharmgkbrs876658928
gwascentralrs876658928
openSNPrs876658928
23andMers876658928
23andMe allrs876658928
SNP Nexus

SNPshotrs876658928
SNPdbers876658928
MSV3drs876658928
GWAS Ctlgrs876658928
Max Magnitude0
ClinVar
Risk rs876658928(;)
Alt rs876658928(;)
Reference rs876658928(TG;TG)
Significance Pathogenic
Disease Tumor susceptibility linked to germline BAP1 mutations Breast-ovarian cancer
Variation info
Gene BRCA2
CLNDBN Tumor susceptibility linked to germline BAP1 mutations Breast-ovarian cancer, familial 2
Reversed 0
HGVS NC_000013.10:g.32911115_32911116delGT
CLNSRC
CLNACC RCV000214776.1, RCV000239057.1,