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rs758972589

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs758972589(A;A)
Make rs758972589(A;G)
ReferenceGRCh38.p2 38.2/144
Chromosome2
Position214792327
GeneBARD1
is asnp
is mentioned by
dbSNPrs758972589
ebirs758972589
HLIrs758972589
Exacrs758972589
Varsomers758972589
Maprs758972589
PheGenIrs758972589
hapmaprs758972589
1000 genomesrs758972589
hgdprs758972589
ensemblrs758972589
gopubmedrs758972589
geneviewrs758972589
scholarrs758972589
googlers758972589
pharmgkbrs758972589
gwascentralrs758972589
openSNPrs758972589
23andMers758972589
23andMe allrs758972589
SNP Nexus

SNPshotrs758972589
SNPdbers758972589
MSV3drs758972589
GWAS Ctlgrs758972589
Max Magnitude0
ClinVar
Risk rs758972589(A;A)
Alt rs758972589(A;A)
Reference rs758972589(G;G)
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 0
HGVS NC_000002.11:g.215657051G>A
CLNSRC
CLNACC RCV000164507.1, RCV000233846.1,