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rs879255323

From SNPedia

Orientationplus
Geno Mag Summary
(AATC;AATC) 0 common in clinvar
Make rs879255323(AATC;CATT)
Make rs879255323(CATT;CATT)
ReferenceGRCh38.p2 38.2/147
Chromosome13
Position32332592
GeneBRCA2
is asnp
is mentioned by
dbSNPrs879255323
ebirs879255323
HLIrs879255323
Exacrs879255323
Varsomers879255323
Maprs879255323
PheGenIrs879255323
hapmaprs879255323
1000 genomesrs879255323
hgdprs879255323
ensemblrs879255323
gopubmedrs879255323
geneviewrs879255323
scholarrs879255323
googlers879255323
pharmgkbrs879255323
gwascentralrs879255323
openSNPrs879255323
23andMers879255323
23andMe allrs879255323
SNP Nexus

SNPshotrs879255323
SNPdbers879255323
MSV3drs879255323
GWAS Ctlgrs879255323
Max Magnitude0
ClinVar
Risk rs879255323(CATT;CATT)
Alt rs879255323(CATT;CATT)
Reference rs879255323(AATC;AATC)
Significance Probable-Pathogenic
Disease Familial cancer of breast
Variation info
Gene BRCA2
CLNDBN Familial cancer of breast
Reversed 0
HGVS NC_000013.10:g.32906729_32906732delAATCinsCATT
CLNSRC
CLNACC RCV000238937.1,