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rs587782028

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs587782028(G;T)
Make rs587782028(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome13
Position32357901
GeneBRCA2
is asnp
is mentioned by
dbSNPrs587782028
ebirs587782028
HLIrs587782028
Exacrs587782028
Varsomers587782028
Maprs587782028
PheGenIrs587782028
hapmaprs587782028
1000 genomesrs587782028
hgdprs587782028
ensemblrs587782028
gopubmedrs587782028
geneviewrs587782028
scholarrs587782028
googlers587782028
pharmgkbrs587782028
gwascentralrs587782028
openSNPrs587782028
23andMers587782028
23andMe allrs587782028
SNP Nexus

SNPshotrs587782028
SNPdbers587782028
MSV3drs587782028
GWAS Ctlgrs587782028
Max Magnitude0
ClinVar
Risk rs587782028(T;T)
Alt rs587782028(T;T)
Reference rs587782028(G;G)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene BRCA2
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000013.10:g.32932038G>T
CLNSRC
CLNACC RCV000130472.2,