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rs879255327

From SNPedia

Orientationplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs879255327(-;-)
Make rs879255327(-;A)
Make rs879255327(A;A)
ReferenceGRCh38.p2 38.2/147
Chromosome13
Position32333299
GeneBRCA2
is asnp
is mentioned by
dbSNPrs879255327
ebirs879255327
HLIrs879255327
Exacrs879255327
Varsomers879255327
Maprs879255327
PheGenIrs879255327
hapmaprs879255327
1000 genomesrs879255327
hgdprs879255327
ensemblrs879255327
gopubmedrs879255327
geneviewrs879255327
scholarrs879255327
googlers879255327
pharmgkbrs879255327
gwascentralrs879255327
openSNPrs879255327
23andMers879255327
23andMe allrs879255327
SNP Nexus

SNPshotrs879255327
SNPdbers879255327
MSV3drs879255327
GWAS Ctlgrs879255327
Max Magnitude0
ClinVar
Risk rs879255327(A;A)
Alt rs879255327(A;A)
Reference rs879255327(;)
Significance Probable-Pathogenic
Disease Familial cancer of breast
Variation info
Gene BRCA2
CLNDBN Familial cancer of breast
Reversed 0
HGVS NC_000013.10:g.32907436dupA
CLNSRC
CLNACC RCV000238765.1,