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rs587782504

From SNPedia

Orientationminus
Geno Mag Summary
(AT;AT) 0 common in clinvar
Make rs587782504(-;-)
Make rs587782504(-;AT)
ReferenceGRCh38.p2 38.2/144
Chromosome2
Position214730479
GeneBARD1
is asnp
is mentioned by
dbSNPrs587782504
ebirs587782504
HLIrs587782504
Exacrs587782504
Varsomers587782504
Maprs587782504
PheGenIrs587782504
hapmaprs587782504
1000 genomesrs587782504
hgdprs587782504
ensemblrs587782504
gopubmedrs587782504
geneviewrs587782504
scholarrs587782504
googlers587782504
pharmgkbrs587782504
gwascentralrs587782504
openSNPrs587782504
23andMers587782504
23andMe allrs587782504
SNP Nexus

SNPshotrs587782504
SNPdbers587782504
MSV3drs587782504
GWAS Ctlgrs587782504
Max Magnitude0
ClinVar
Risk rs587782504(;)
Alt rs587782504(;)
Reference rs587782504(AT;AT)
Significance Other
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene BARD1
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 1
HGVS NC_000002.11:g.215595203_215595204delAT
CLNSRC
CLNACC RCV000131644.3,