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

rs587779364

From SNPedia

Orientationplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs587779364(-;-)
Make rs587779364(-;C)
Make rs587779364(C;C)
ReferenceGRCh38.p2 38.2/144
Chromosome13
Position32339719
GeneBRCA2
is asnp
is mentioned by
dbSNPrs587779364
ebirs587779364
HLIrs587779364
Exacrs587779364
Varsomers587779364
Maprs587779364
PheGenIrs587779364
hapmaprs587779364
1000 genomesrs587779364
hgdprs587779364
ensemblrs587779364
gopubmedrs587779364
geneviewrs587779364
scholarrs587779364
googlers587779364
pharmgkbrs587779364
gwascentralrs587779364
openSNPrs587779364
23andMers587779364
23andMe allrs587779364
SNP Nexus

SNPshotrs587779364
SNPdbers587779364
MSV3drs587779364
GWAS Ctlgrs587779364
Max Magnitude0
ClinVar
Risk rs587779364(C;C)
Alt rs587779364(C;C)
Reference rs587779364(;)
Significance Pathogenic
Disease Familial cancer of breast
Variation info
Gene BRCA2
CLNDBN Familial cancer of breast
Reversed 0
HGVS NC_000013.10:g.32913856dupC
CLNSRC
CLNACC RCV000074538.3,