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rs587782022

From SNPedia

Orientationplus
Geno Mag Summary
(TG;TG) 0 common in clinvar
Make rs587782022(-;-)
Make rs587782022(-;TG)
ReferenceGRCh38.p2 38.2/144
Chromosome13
Position32337531
GeneBRCA2
is asnp
is mentioned by
dbSNPrs587782022
ebirs587782022
HLIrs587782022
Exacrs587782022
Varsomers587782022
Maprs587782022
PheGenIrs587782022
hapmaprs587782022
1000 genomesrs587782022
hgdprs587782022
ensemblrs587782022
gopubmedrs587782022
geneviewrs587782022
scholarrs587782022
googlers587782022
pharmgkbrs587782022
gwascentralrs587782022
openSNPrs587782022
23andMers587782022
23andMe allrs587782022
SNP Nexus

SNPshotrs587782022
SNPdbers587782022
MSV3drs587782022
GWAS Ctlgrs587782022
Max Magnitude0
ClinVar
Risk rs587782022(;)
Alt rs587782022(;)
Reference rs587782022(TG;TG)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene BRCA2
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000013.10:g.32911668_32911669delTG
CLNSRC
CLNACC RCV000130451.2,