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rs879255306

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(-;T) 6 BRCA2 variant considered pathogenic for breast cancer
(T;T) 0 common in clinvar


Make rs879255306(-;-)
ReferenceGRCh38.p2 38.2/147
Chromosome13
Position32346869
GeneBRCA2
is asnp
is mentioned by
dbSNPrs879255306
dbSNP (old)rs879255306
ClinGenrs879255306
ebirs879255306
HLIrs879255306
Exacrs879255306
Gnomadrs879255306
Varsomers879255306
Maprs879255306
PheGenIrs879255306
Biobankrs879255306
1000 genomesrs879255306
hgdprs879255306
ensemblrs879255306
gopubmedrs879255306
geneviewrs879255306
scholarrs879255306
googlers879255306
pharmgkbrs879255306
gwascentralrs879255306
openSNPrs879255306
23andMers879255306
23andMe allrs879255306
SNP Nexus

SNPshotrs879255306
SNPdbers879255306
MSV3drs879255306
GWAS Ctlgrs879255306
Max Magnitude6
ClinVar
Risk rs879255306(-;-)
Alt rs879255306(-;-)
Reference Rs879255306(T;T)
Significance Pathogenic
Disease Breast-ovarian cancer not provided
Variation info
Gene BRCA2
CLNDBN Breast-ovarian cancer, familial 2 not provided
Reversed 0
HGVS NC_000013.10:g.32921006delT
CLNSRC
CLNACC RCV000238627.2, RCV000482674.1,