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

rs587782598

From SNPedia

Orientationplus
Geno Mag Summary
(AG;AG) 0 common in clinvar
Make rs587782598(-;-)
Make rs587782598(-;GA)
Make rs587782598(GA;GA)
ReferenceGRCh38.p2 38.2/144
Chromosome13
Position32339741
GeneBRCA2
is asnp
is mentioned by
dbSNPrs587782598
ebirs587782598
HLIrs587782598
Exacrs587782598
Varsomers587782598
Maprs587782598
PheGenIrs587782598
hapmaprs587782598
1000 genomesrs587782598
hgdprs587782598
ensemblrs587782598
gopubmedrs587782598
geneviewrs587782598
scholarrs587782598
googlers587782598
pharmgkbrs587782598
gwascentralrs587782598
openSNPrs587782598
23andMers587782598
23andMe allrs587782598
SNP Nexus

SNPshotrs587782598
SNPdbers587782598
MSV3drs587782598
GWAS Ctlgrs587782598
Max Magnitude0
ClinVar
Risk rs587782598(;)
Alt rs587782598(;)
Reference rs587782598(AG;AG)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome Breast-ovarian cancer
Variation info
Gene BRCA2
CLNDBN Hereditary cancer-predisposing syndrome Breast-ovarian cancer, familial 2
Reversed 0
HGVS NC_000013.10:g.32913878_32913879delGA
CLNSRC
CLNACC RCV000131950.2, RCV000239140.1,