Have questions? Visit https://www.reddit.com/r/SNPedia

rs879255321

From SNPedia

Orientationplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs879255321(-;-)
Make rs879255321(-;A)
Make rs879255321(A;A)
ReferenceGRCh38.p2 38.2/147
Chromosome13
Position32325137
GeneBRCA2
is asnp
is mentioned by
dbSNPrs879255321
ebirs879255321
HLIrs879255321
Exacrs879255321
Varsomers879255321
Maprs879255321
PheGenIrs879255321
hapmaprs879255321
1000 genomesrs879255321
hgdprs879255321
ensemblrs879255321
gopubmedrs879255321
geneviewrs879255321
scholarrs879255321
googlers879255321
pharmgkbrs879255321
gwascentralrs879255321
openSNPrs879255321
23andMers879255321
23andMe allrs879255321
SNP Nexus

SNPshotrs879255321
SNPdbers879255321
MSV3drs879255321
GWAS Ctlgrs879255321
Max Magnitude0
ClinVar
Risk rs879255321(A;A)
Alt rs879255321(A;A)
Reference rs879255321(;)
Significance Probable-Pathogenic
Disease not specified
Variation info
Gene BRCA2
CLNDBN not specified
Reversed 0
HGVS NC_000013.10:g.32899274dupA
CLNSRC
CLNACC RCV000239216.1,