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rs587782897

From SNPedia

Orientationminus
Geno Mag Summary
(AT;AT) 0 common in clinvar
Make rs587782897(-;-)
Make rs587782897(-;AT)
ReferenceGRCh38.p2 38.2/144
Chromosome2
Position214745152
GeneBARD1
is asnp
is mentioned by
dbSNPrs587782897
ebirs587782897
HLIrs587782897
Exacrs587782897
Varsomers587782897
Maprs587782897
PheGenIrs587782897
hapmaprs587782897
1000 genomesrs587782897
hgdprs587782897
ensemblrs587782897
gopubmedrs587782897
geneviewrs587782897
scholarrs587782897
googlers587782897
pharmgkbrs587782897
gwascentralrs587782897
openSNPrs587782897
23andMers587782897
23andMe allrs587782897
SNP Nexus

SNPshotrs587782897
SNPdbers587782897
MSV3drs587782897
GWAS Ctlgrs587782897
Max Magnitude0
ClinVar
Risk rs587782897(;)
Alt rs587782897(;)
Reference rs587782897(AT;AT)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene BARD1
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 1
HGVS NC_000002.11:g.215609876_215609877delAT
CLNSRC
CLNACC RCV000132536.2,