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rs587781728

From SNPedia

Orientationminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs587781728(G;G)
Make rs587781728(G;T)
ReferenceGRCh38.p2 38.2/144
Chromosome2
Position214780927
GeneBARD1
is asnp
is mentioned by
dbSNPrs587781728
ebirs587781728
HLIrs587781728
Exacrs587781728
Varsomers587781728
Maprs587781728
PheGenIrs587781728
hapmaprs587781728
1000 genomesrs587781728
hgdprs587781728
ensemblrs587781728
gopubmedrs587781728
geneviewrs587781728
scholarrs587781728
googlers587781728
pharmgkbrs587781728
gwascentralrs587781728
openSNPrs587781728
23andMers587781728
23andMe allrs587781728
SNP Nexus

SNPshotrs587781728
SNPdbers587781728
MSV3drs587781728
GWAS Ctlgrs587781728
Max Magnitude0
ClinVar
Risk rs587781728(G;G)
Alt rs587781728(G;G)
Reference rs587781728(T;T)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene BARD1
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 1
HGVS NC_000002.11:g.215645651A>C
CLNSRC
CLNACC RCV000129918.2,