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rs879255322

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs879255322(-;-)
Make rs879255322(-;T)
ReferenceGRCh38.p2 38.2/147
Chromosome13
Position32332535
GeneBRCA2
is asnp
is mentioned by
dbSNPrs879255322
ebirs879255322
HLIrs879255322
Exacrs879255322
Varsomers879255322
Maprs879255322
PheGenIrs879255322
hapmaprs879255322
1000 genomesrs879255322
hgdprs879255322
ensemblrs879255322
gopubmedrs879255322
geneviewrs879255322
scholarrs879255322
googlers879255322
pharmgkbrs879255322
gwascentralrs879255322
openSNPrs879255322
23andMers879255322
23andMe allrs879255322
SNP Nexus

SNPshotrs879255322
SNPdbers879255322
MSV3drs879255322
GWAS Ctlgrs879255322
Max Magnitude0
ClinVar
Risk rs879255322(;)
Alt rs879255322(;)
Reference rs879255322(T;T)
Significance Probable-Pathogenic
Disease Familial cancer of breast
Variation info
Gene BRCA2
CLNDBN Familial cancer of breast
Reversed 0
HGVS NC_000013.10:g.32906672delT
CLNSRC
CLNACC RCV000238640.1,