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

rs587781849

From SNPedia

Orientationplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs587781849(-;-)
Make rs587781849(-;T)
Make rs587781849(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome13
Position32339717
GeneBRCA2
is asnp
is mentioned by
dbSNPrs587781849
ebirs587781849
HLIrs587781849
Exacrs587781849
Varsomers587781849
Maprs587781849
PheGenIrs587781849
hapmaprs587781849
1000 genomesrs587781849
hgdprs587781849
ensemblrs587781849
gopubmedrs587781849
geneviewrs587781849
scholarrs587781849
googlers587781849
pharmgkbrs587781849
gwascentralrs587781849
openSNPrs587781849
23andMers587781849
23andMe allrs587781849
SNP Nexus

SNPshotrs587781849
SNPdbers587781849
MSV3drs587781849
GWAS Ctlgrs587781849
Max Magnitude0
ClinVar
Risk rs587781849(T;T)
Alt rs587781849(T;T)
Reference rs587781849(;)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene BRCA2
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000013.10:g.32913854dupT
CLNSRC
CLNACC RCV000130153.2,