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rs587782095

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs587782095(G;G)
Make rs587782095(G;T)
ReferenceGRCh38.p2 38.2/144
Chromosome13
Position32336667
GeneBRCA2
is asnp
is mentioned by
dbSNPrs587782095
ebirs587782095
HLIrs587782095
Exacrs587782095
Varsomers587782095
Maprs587782095
PheGenIrs587782095
hapmaprs587782095
1000 genomesrs587782095
hgdprs587782095
ensemblrs587782095
gopubmedrs587782095
geneviewrs587782095
scholarrs587782095
googlers587782095
pharmgkbrs587782095
gwascentralrs587782095
openSNPrs587782095
23andMers587782095
23andMe allrs587782095
SNP Nexus

SNPshotrs587782095
SNPdbers587782095
MSV3drs587782095
GWAS Ctlgrs587782095
Max Magnitude0
ClinVar
Risk rs587782095(G;G)
Alt rs587782095(G;G)
Reference rs587782095(T;T)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene BRCA2
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000013.10:g.32910804T>G
CLNSRC
CLNACC RCV000130606.2,