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rs876659770

From SNPedia

Orientationplus
Geno Mag Summary
(CAAA;CAAA) 0 common in clinvar
Make rs876659770(CAAA;GG)
Make rs876659770(GG;GG)
ReferenceGRCh38.p2 38.2/147
Chromosome13
Position32355062
GeneBRCA2
is asnp
is mentioned by
dbSNPrs876659770
ebirs876659770
HLIrs876659770
Exacrs876659770
Varsomers876659770
Maprs876659770
PheGenIrs876659770
hapmaprs876659770
1000 genomesrs876659770
hgdprs876659770
ensemblrs876659770
gopubmedrs876659770
geneviewrs876659770
scholarrs876659770
googlers876659770
pharmgkbrs876659770
gwascentralrs876659770
openSNPrs876659770
23andMers876659770
23andMe allrs876659770
SNP Nexus

SNPshotrs876659770
SNPdbers876659770
MSV3drs876659770
GWAS Ctlgrs876659770
Max Magnitude0
ClinVar
Risk rs876659770(GG;GG)
Alt rs876659770(GG;GG)
Reference rs876659770(CAAA;CAAA)
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.32929199_32929202delCAAAinsGG
CLNSRC
CLNACC RCV000218396.1,