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

rs587782667

From SNPedia

Orientationplus
Geno Mag Summary
(TA;TA) 0 common in clinvar
Make rs587782667(-;-)
Make rs587782667(-;AT)
Make rs587782667(AT;AT)
ReferenceGRCh38.p2 38.2/144
Chromosome13
Position32341058
GeneBRCA2
is asnp
is mentioned by
dbSNPrs587782667
ebirs587782667
HLIrs587782667
Exacrs587782667
Varsomers587782667
Maprs587782667
PheGenIrs587782667
hapmaprs587782667
1000 genomesrs587782667
hgdprs587782667
ensemblrs587782667
gopubmedrs587782667
geneviewrs587782667
scholarrs587782667
googlers587782667
pharmgkbrs587782667
gwascentralrs587782667
openSNPrs587782667
23andMers587782667
23andMe allrs587782667
SNP Nexus

SNPshotrs587782667
SNPdbers587782667
MSV3drs587782667
GWAS Ctlgrs587782667
Max Magnitude0
ClinVar
Risk rs587782667(;)
Alt rs587782667(;)
Reference rs587782667(TA;TA)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene BRCA2
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000013.10:g.32915195_32915196delAT
CLNSRC
CLNACC RCV000132088.2,