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rs879255328

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs879255328(-;-)
Make rs879255328(-;A)
ReferenceGRCh38.p2 38.2/147
Chromosome13
Position32339124
GeneBRCA2
is asnp
is mentioned by
dbSNPrs879255328
ebirs879255328
HLIrs879255328
Exacrs879255328
Varsomers879255328
Maprs879255328
PheGenIrs879255328
hapmaprs879255328
1000 genomesrs879255328
hgdprs879255328
ensemblrs879255328
gopubmedrs879255328
geneviewrs879255328
scholarrs879255328
googlers879255328
pharmgkbrs879255328
gwascentralrs879255328
openSNPrs879255328
23andMers879255328
23andMe allrs879255328
SNP Nexus

SNPshotrs879255328
SNPdbers879255328
MSV3drs879255328
GWAS Ctlgrs879255328
Max Magnitude0
ClinVar
Risk rs879255328(;)
Alt rs879255328(;)
Reference rs879255328(A;A)
Significance Probable-Pathogenic
Disease Familial cancer of breast
Variation info
Gene BRCA2
CLNDBN Familial cancer of breast
Reversed 0
HGVS NC_000013.10:g.32913261delA
CLNSRC
CLNACC RCV000238636.1,