rs876659560

Orientation

minus

Stabilized

minus

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

Make rs876659560(-;-)

Make rs876659560(-;A)

Reference

GRCh38.p2 38.2/147

Chromosome

2

Position

214730510

Gene

BARD1

is a	snp
is	mentioned by
dbSNP	rs876659560
dbSNP (classic)	rs876659560
ClinGen	rs876659560
ebi	rs876659560
HLI	rs876659560
Exac	rs876659560
Gnomad	rs876659560
Varsome	rs876659560
LitVar	rs876659560
Map	rs876659560
PheGenI	rs876659560
Biobank	rs876659560
1000 genomes	rs876659560
hgdp	rs876659560
ensembl	rs876659560
geneview	rs876659560
scholar	rs876659560
google	rs876659560
pharmgkb	rs876659560
gwascentral	rs876659560
openSNP	rs876659560
23andMe	rs876659560
SNPshot	rs876659560
SNPdbe	rs876659560
MSV3d	rs876659560
GWAS Ctlg	rs876659560

Max Magnitude

0

ClinVar
Risk	rs876659560(-;-)
Alt	rs876659560(-;-)
Reference	Rs876659560(A;A)
Significance	Probable-Pathogenic
Disease	Hereditary cancer-predisposing syndrome
Variation	info
Gene	BARD1
CLNDBN	Hereditary cancer-predisposing syndrome
Reversed	1
HGVS	NC_000002.11:g.215595234delT
CLNSRC
CLNACC	RCV000217479.1,