rs587781728

Orientation

minus

Stabilized

minus

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

Make rs587781728(G;G)

Make rs587781728(G;T)

Reference

GRCh38.p2 38.2/144

Chromosome

2

Position

214780927

Gene

BARD1

is a	snp
is	mentioned by
dbSNP	rs587781728
dbSNP (classic)	rs587781728
ClinGen	rs587781728
ebi	rs587781728
HLI	rs587781728
Exac	rs587781728
Gnomad	rs587781728
Varsome	rs587781728
LitVar	rs587781728
Map	rs587781728
PheGenI	rs587781728
Biobank	rs587781728
1000 genomes	rs587781728
hgdp	rs587781728
ensembl	rs587781728
geneview	rs587781728
scholar	rs587781728
google	rs587781728
pharmgkb	rs587781728
gwascentral	rs587781728
openSNP	rs587781728
23andMe	rs587781728
SNPshot	rs587781728
SNPdbe	rs587781728
MSV3d	rs587781728
GWAS Ctlg	rs587781728

Max Magnitude

0

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,