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rs587781430

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs587781430(C;T)
Make rs587781430(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome2
Position214781141
GeneBARD1
is asnp
is mentioned by
dbSNPrs587781430
ebirs587781430
HLIrs587781430
Exacrs587781430
Varsomers587781430
Maprs587781430
PheGenIrs587781430
hapmaprs587781430
1000 genomesrs587781430
hgdprs587781430
ensemblrs587781430
gopubmedrs587781430
geneviewrs587781430
scholarrs587781430
googlers587781430
pharmgkbrs587781430
gwascentralrs587781430
openSNPrs587781430
23andMers587781430
23andMe allrs587781430
SNP Nexus

SNPshotrs587781430
SNPdbers587781430
MSV3drs587781430
GWAS Ctlgrs587781430
Max Magnitude0
ClinVar
Risk rs587781430(T;T)
Alt rs587781430(T;T)
Reference rs587781430(C;C)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene BARD1
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 1
HGVS NC_000002.11:g.215645865G>A
CLNSRC
CLNACC RCV000129318.2,