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rs587782398

From SNPedia

Orientationplus
Geno Mag Summary
(AT;AT) 0 common in clinvar
Make rs587782398(-;-)
Make rs587782398(-;AT)
ReferenceGRCh38.p2 38.2/144
Chromosome13
Position32326554
GeneBRCA2
is asnp
is mentioned by
dbSNPrs587782398
ebirs587782398
HLIrs587782398
Exacrs587782398
Varsomers587782398
Maprs587782398
PheGenIrs587782398
hapmaprs587782398
1000 genomesrs587782398
hgdprs587782398
ensemblrs587782398
gopubmedrs587782398
geneviewrs587782398
scholarrs587782398
googlers587782398
pharmgkbrs587782398
gwascentralrs587782398
openSNPrs587782398
23andMers587782398
23andMe allrs587782398
SNP Nexus

SNPshotrs587782398
SNPdbers587782398
MSV3drs587782398
GWAS Ctlgrs587782398
Max Magnitude0
ClinVar
Risk rs587782398(;)
Alt rs587782398(;)
Reference rs587782398(AT;AT)
Significance Pathogenic
Disease Breast-ovarian cancer Familial cancer of breast Hereditary cancer-predisposing syndrome not provided
Variation info
Gene BRCA2
CLNDBN Breast-ovarian cancer, familial 2 Familial cancer of breast Hereditary cancer-predisposing syndrome not provided
Reversed 0
HGVS NC_000013.10:g.32900693_32900694delAT
CLNSRC Breast Cancer Information Core (BRCA2)
CLNACC RCV000031574.5, RCV000044741.4, RCV000131852.3, RCV000235138.1,