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rs587781671

From SNPedia

Orientationminus
Geno Mag Summary
(TTTA;TTTA) 0 common in clinvar
Make rs587781671(-;-)
Make rs587781671(-;TTTA)
ReferenceGRCh38.p2 38.2/144
Chromosome2
Position214781214
GeneBARD1
is asnp
is mentioned by
dbSNPrs587781671
ebirs587781671
HLIrs587781671
Exacrs587781671
Varsomers587781671
Maprs587781671
PheGenIrs587781671
hapmaprs587781671
1000 genomesrs587781671
hgdprs587781671
ensemblrs587781671
gopubmedrs587781671
geneviewrs587781671
scholarrs587781671
googlers587781671
pharmgkbrs587781671
gwascentralrs587781671
openSNPrs587781671
23andMers587781671
23andMe allrs587781671
SNP Nexus

SNPshotrs587781671
SNPdbers587781671
MSV3drs587781671
GWAS Ctlgrs587781671
Max Magnitude0
ClinVar
Risk rs587781671(;)
Alt rs587781671(;)
Reference rs587781671(TTTA;TTTA)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene BARD1
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 1
HGVS NC_000002.11:g.215645938_215645941delTAAA
CLNSRC
CLNACC RCV000129827.2,