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rs587782612

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;T) 6 BRCA2 variant considered pathogenic for breast cancer
(T;T) 0 common in clinvar


Make rs587782612(A;A)
ReferenceGRCh38.p2 38.2/144
Chromosome13
Position32396957
GeneBRCA2
is asnp
is mentioned by
dbSNPrs587782612
dbSNP (classic)rs587782612
ClinGenrs587782612
ebirs587782612
HLIrs587782612
Exacrs587782612
Gnomadrs587782612
Varsomers587782612
LitVarrs587782612
Maprs587782612
PheGenIrs587782612
Biobankrs587782612
1000 genomesrs587782612
hgdprs587782612
ensemblrs587782612
geneviewrs587782612
scholarrs587782612
googlers587782612
pharmgkbrs587782612
gwascentralrs587782612
openSNPrs587782612
23andMers587782612
SNPshotrs587782612
SNPdbers587782612
MSV3drs587782612
GWAS Ctlgrs587782612
Max Magnitude6
ClinVar
Risk rs587782612(A;A)
Alt rs587782612(A;A)
Reference Rs587782612(T;T)
Significance Probable-Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene BRCA2
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000013.10:g.32971094T>A
CLNSRC
CLNACC RCV000131987.3,