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

rs879255324

From SNPedia

Orientationplus
Geno Mag Summary
(AA;AA) 0 common in clinvar
Make rs879255324(-;-)
Make rs879255324(-;AA)
ReferenceGRCh38.p2 38.2/147
Chromosome13
Position32332784
GeneBRCA2
is asnp
is mentioned by
dbSNPrs879255324
ebirs879255324
HLIrs879255324
Exacrs879255324
Varsomers879255324
Maprs879255324
PheGenIrs879255324
hapmaprs879255324
1000 genomesrs879255324
hgdprs879255324
ensemblrs879255324
gopubmedrs879255324
geneviewrs879255324
scholarrs879255324
googlers879255324
pharmgkbrs879255324
gwascentralrs879255324
openSNPrs879255324
23andMers879255324
23andMe allrs879255324
SNP Nexus

SNPshotrs879255324
SNPdbers879255324
MSV3drs879255324
GWAS Ctlgrs879255324
Max Magnitude0
ClinVar
Risk rs879255324(;)
Alt rs879255324(;)
Reference rs879255324(AA;AA)
Significance Probable-Pathogenic
Disease not specified
Variation info
Gene BRCA2
CLNDBN not specified
Reversed 0
HGVS NC_000013.10:g.32906921_32906922delAA
CLNSRC
CLNACC RCV000239225.1,