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rs879255326

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs879255326(-;-)
Make rs879255326(-;G)
ReferenceGRCh38.p2 38.2/147
Chromosome13
Position32333211
GeneBRCA2
is asnp
is mentioned by
dbSNPrs879255326
ebirs879255326
HLIrs879255326
Exacrs879255326
Varsomers879255326
Maprs879255326
PheGenIrs879255326
hapmaprs879255326
1000 genomesrs879255326
hgdprs879255326
ensemblrs879255326
gopubmedrs879255326
geneviewrs879255326
scholarrs879255326
googlers879255326
pharmgkbrs879255326
gwascentralrs879255326
openSNPrs879255326
23andMers879255326
23andMe allrs879255326
SNP Nexus

SNPshotrs879255326
SNPdbers879255326
MSV3drs879255326
GWAS Ctlgrs879255326
Max Magnitude0
ClinVar
Risk rs879255326(;)
Alt rs879255326(;)
Reference rs879255326(G;G)
Significance Probable-Pathogenic
Disease Familial cancer of breast
Variation info
Gene BRCA2
CLNDBN Familial cancer of breast
Reversed 0
HGVS NC_000013.10:g.32907348delG
CLNSRC
CLNACC RCV000239261.1,