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rs587782010

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs587782010(C;T)
Make rs587782010(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome13
Position32371076
GeneBRCA2
is asnp
is mentioned by
dbSNPrs587782010
ebirs587782010
HLIrs587782010
Exacrs587782010
Varsomers587782010
Maprs587782010
PheGenIrs587782010
hapmaprs587782010
1000 genomesrs587782010
hgdprs587782010
ensemblrs587782010
gopubmedrs587782010
geneviewrs587782010
scholarrs587782010
googlers587782010
pharmgkbrs587782010
gwascentralrs587782010
openSNPrs587782010
23andMers587782010
23andMe allrs587782010
SNP Nexus

SNPshotrs587782010
SNPdbers587782010
MSV3drs587782010
GWAS Ctlgrs587782010
Max Magnitude0
ClinVar
Risk rs587782010(T;T)
Alt rs587782010(T;T)
Reference rs587782010(C;C)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene BRCA2
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000013.10:g.32945213C>T
CLNSRC
CLNACC RCV000130433.2,