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rs876658425

From SNPedia

Orientationplus
Geno Mag Summary
(GCATAGTC;GCATAGTC) 0 common in clinvar
Make rs876658425(-;-)
Make rs876658425(-;GCATAGTC)
ReferenceGRCh38.p2 38.2/147
Chromosome13
Position32340622
GeneBRCA2
is asnp
is mentioned by
dbSNPrs876658425
ebirs876658425
HLIrs876658425
Exacrs876658425
Varsomers876658425
Maprs876658425
PheGenIrs876658425
hapmaprs876658425
1000 genomesrs876658425
hgdprs876658425
ensemblrs876658425
gopubmedrs876658425
geneviewrs876658425
scholarrs876658425
googlers876658425
pharmgkbrs876658425
gwascentralrs876658425
openSNPrs876658425
23andMers876658425
23andMe allrs876658425
SNP Nexus

SNPshotrs876658425
SNPdbers876658425
MSV3drs876658425
GWAS Ctlgrs876658425
Max Magnitude0
ClinVar
Risk rs876658425(;)
Alt rs876658425(;)
Reference rs876658425(GCATAGTC;GCATAGTC)
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.32914759_32914766delGCATAGTC
CLNSRC
CLNACC RCV000216272.1,