rs587781671

Orientation

minus

Stabilized

minus

Geno	Mag	Summary
(TTTA;TTTA)	0	common in clinvar

Make rs587781671(-;-)

Make rs587781671(-;TTTA)

Reference

GRCh38.p2 38.2/144

Chromosome

2

Position

214781214

Gene

BARD1

is a	snp
is	mentioned by
dbSNP	rs587781671
dbSNP (classic)	rs587781671
ClinGen	rs587781671
ebi	rs587781671
HLI	rs587781671
Exac	rs587781671
Gnomad	rs587781671
Varsome	rs587781671
LitVar	rs587781671
Map	rs587781671
PheGenI	rs587781671
Biobank	rs587781671
1000 genomes	rs587781671
hgdp	rs587781671
ensembl	rs587781671
geneview	rs587781671
scholar	rs587781671
google	rs587781671
pharmgkb	rs587781671
gwascentral	rs587781671
openSNP	rs587781671
23andMe	rs587781671
SNPshot	rs587781671
SNPdbe	rs587781671
MSV3d	rs587781671
GWAS Ctlg	rs587781671

Max Magnitude

0

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,