rs587781430

Orientation

minus

Stabilized

minus

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

Make rs587781430(C;T)

Make rs587781430(T;T)

Reference

GRCh38.p2 38.2/144

Chromosome

2

Position

214781141

Gene

BARD1

is a	snp
is	mentioned by
dbSNP	rs587781430
dbSNP (classic)	rs587781430
ClinGen	rs587781430
ebi	rs587781430
HLI	rs587781430
Exac	rs587781430
Gnomad	rs587781430
Varsome	rs587781430
LitVar	rs587781430
Map	rs587781430
PheGenI	rs587781430
Biobank	rs587781430
1000 genomes	rs587781430
hgdp	rs587781430
ensembl	rs587781430
geneview	rs587781430
scholar	rs587781430
google	rs587781430
pharmgkb	rs587781430
gwascentral	rs587781430
openSNP	rs587781430
23andMe	rs587781430
SNPshot	rs587781430
SNPdbe	rs587781430
MSV3d	rs587781430
GWAS Ctlg	rs587781430

Max Magnitude

0

ClinVar
Risk	rs587781430(T;T)
Alt	rs587781430(T;T)
Reference	Rs587781430(C;C)
Significance	Pathogenic
Disease	Hereditary cancer-predisposing syndrome not provided
Variation	info
Gene	BARD1
CLNDBN	Hereditary cancer-predisposing syndrome not provided
Reversed	1
HGVS	NC_000002.11:g.215645865G>A
CLNSRC
CLNACC	RCV000129318.2, RCV000480724.1,