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rs879255332

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs879255332(-;-)
Make rs879255332(-;T)
ReferenceGRCh38.p2 38.2/147
Chromosome13
Position32362631
GeneBRCA2
is asnp
is mentioned by
dbSNPrs879255332
ebirs879255332
HLIrs879255332
Exacrs879255332
Varsomers879255332
Maprs879255332
PheGenIrs879255332
hapmaprs879255332
1000 genomesrs879255332
hgdprs879255332
ensemblrs879255332
gopubmedrs879255332
geneviewrs879255332
scholarrs879255332
googlers879255332
pharmgkbrs879255332
gwascentralrs879255332
openSNPrs879255332
23andMers879255332
23andMe allrs879255332
SNP Nexus

SNPshotrs879255332
SNPdbers879255332
MSV3drs879255332
GWAS Ctlgrs879255332
Max Magnitude0
ClinVar
Risk rs879255332(;)
Alt rs879255332(;)
Reference rs879255332(T;T)
Significance Probable-Pathogenic
Disease not specified
Variation info
Gene BRCA2
CLNDBN not specified
Reversed 0
HGVS NC_000013.10:g.32936768delT
CLNSRC
CLNACC RCV000238889.1,