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rs876659154

From SNPedia

Orientationplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs876659154(-;-)
Make rs876659154(-;A)
Make rs876659154(A;A)
ReferenceGRCh38.p2 38.2/147
Chromosome13
Position32337190
GeneBRCA2
is asnp
is mentioned by
dbSNPrs876659154
ebirs876659154
HLIrs876659154
Exacrs876659154
Varsomers876659154
Maprs876659154
PheGenIrs876659154
hapmaprs876659154
1000 genomesrs876659154
hgdprs876659154
ensemblrs876659154
gopubmedrs876659154
geneviewrs876659154
scholarrs876659154
googlers876659154
pharmgkbrs876659154
gwascentralrs876659154
openSNPrs876659154
23andMers876659154
23andMe allrs876659154
SNP Nexus

SNPshotrs876659154
SNPdbers876659154
MSV3drs876659154
GWAS Ctlgrs876659154
Max Magnitude0
ClinVar
Risk rs876659154(A;A)
Alt rs876659154(A;A)
Reference rs876659154(;)
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.32911327dupA
CLNSRC
CLNACC RCV000222494.1,