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rs876658631

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs876658631(C;T)
Make rs876658631(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome13
Position32356508
GeneBRCA2
is asnp
is mentioned by
dbSNPrs876658631
ebirs876658631
HLIrs876658631
Exacrs876658631
Varsomers876658631
Maprs876658631
PheGenIrs876658631
hapmaprs876658631
1000 genomesrs876658631
hgdprs876658631
ensemblrs876658631
gopubmedrs876658631
geneviewrs876658631
scholarrs876658631
googlers876658631
pharmgkbrs876658631
gwascentralrs876658631
openSNPrs876658631
23andMers876658631
23andMe allrs876658631
SNP Nexus

SNPshotrs876658631
SNPdbers876658631
MSV3drs876658631
GWAS Ctlgrs876658631
Max Magnitude0
ClinVar
Risk rs876658631(T;T)
Alt rs876658631(T;T)
Reference rs876658631(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.32930645C>T
CLNSRC
CLNACC RCV000215458.1,