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rs587780021

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs587780021(C;T)
Make rs587780021(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome2
Position214745842
GeneBARD1
is asnp
is mentioned by
dbSNPrs587780021
ebirs587780021
HLIrs587780021
Exacrs587780021
Varsomers587780021
Maprs587780021
PheGenIrs587780021
hapmaprs587780021
1000 genomesrs587780021
hgdprs587780021
ensemblrs587780021
gopubmedrs587780021
geneviewrs587780021
scholarrs587780021
googlers587780021
pharmgkbrs587780021
gwascentralrs587780021
openSNPrs587780021
23andMers587780021
23andMe allrs587780021
SNP Nexus

SNPshotrs587780021
SNPdbers587780021
MSV3drs587780021
GWAS Ctlgrs587780021
Max Magnitude0
ClinVar
Risk rs587780021(T;T)
Alt rs587780021(T;T)
Reference rs587780021(C;C)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome Familial cancer of breast not provided
Variation info
Gene BARD1
CLNDBN Hereditary cancer-predisposing syndrome Familial cancer of breast not provided
Reversed 1
HGVS NC_000002.11:g.215610566G>A
CLNSRC
CLNACC RCV000115616.4, RCV000205536.2, RCV000212135.1,