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rs876659345

From SNPedia

Orientationplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs876659345(-;-)
Make rs876659345(-;T)
Make rs876659345(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome13
Position32355071
GeneBRCA2
is asnp
is mentioned by
dbSNPrs876659345
ebirs876659345
HLIrs876659345
Exacrs876659345
Varsomers876659345
Maprs876659345
PheGenIrs876659345
hapmaprs876659345
1000 genomesrs876659345
hgdprs876659345
ensemblrs876659345
gopubmedrs876659345
geneviewrs876659345
scholarrs876659345
googlers876659345
pharmgkbrs876659345
gwascentralrs876659345
openSNPrs876659345
23andMers876659345
23andMe allrs876659345
SNP Nexus

SNPshotrs876659345
SNPdbers876659345
MSV3drs876659345
GWAS Ctlgrs876659345
Max Magnitude0
ClinVar
Risk rs876659345(T;T)
Alt rs876659345(T;T)
Reference rs876659345(;)
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.32929208dupT
CLNSRC
CLNACC RCV000219382.1,