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rs587782681

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs587782681(C;G)
Make rs587782681(G;G)
ReferenceGRCh38.p2 38.2/144
Chromosome2
Position214780662
GeneBARD1
is asnp
is mentioned by
dbSNPrs587782681
ebirs587782681
HLIrs587782681
Exacrs587782681
Varsomers587782681
Maprs587782681
PheGenIrs587782681
hapmaprs587782681
1000 genomesrs587782681
hgdprs587782681
ensemblrs587782681
gopubmedrs587782681
geneviewrs587782681
scholarrs587782681
googlers587782681
pharmgkbrs587782681
gwascentralrs587782681
openSNPrs587782681
23andMers587782681
23andMe allrs587782681
SNP Nexus

SNPshotrs587782681
SNPdbers587782681
MSV3drs587782681
GWAS Ctlgrs587782681
Max Magnitude0
ClinVar
Risk rs587782681(G;G)
Alt rs587782681(G;G)
Reference rs587782681(C;C)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome Familial cancer of breast
Variation info
Gene BARD1
CLNDBN Hereditary cancer-predisposing syndrome Familial cancer of breast
Reversed 1
HGVS NC_000002.11:g.215645386G>C
CLNSRC
CLNACC RCV000132107.2, RCV000195626.1,