rs786203891

Orientation

minus

Stabilized

minus

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

Make rs786203891(-;-)

Make rs786203891(-;A)

Reference

GRCh38.p2 38.2/146

Chromosome

2

Position

214780676

Gene

BARD1

is a	snp
is	mentioned by
dbSNP	rs786203891
dbSNP (classic)	rs786203891
ClinGen	rs786203891
ebi	rs786203891
HLI	rs786203891
Exac	rs786203891
Gnomad	rs786203891
Varsome	rs786203891
LitVar	rs786203891
Map	rs786203891
PheGenI	rs786203891
Biobank	rs786203891
1000 genomes	rs786203891
hgdp	rs786203891
ensembl	rs786203891
geneview	rs786203891
scholar	rs786203891
google	rs786203891
pharmgkb	rs786203891
gwascentral	rs786203891
openSNP	rs786203891
23andMe	rs786203891
SNPshot	rs786203891
SNPdbe	rs786203891
MSV3d	rs786203891
GWAS Ctlg	rs786203891

Max Magnitude

0

ClinVar
Risk	rs786203891(-;-)
Alt	rs786203891(-;-)
Reference	Rs786203891(A;A)
Significance	Pathogenic
Disease	Hereditary cancer-predisposing syndrome
Variation	info
Gene	BARD1
CLNDBN	Hereditary cancer-predisposing syndrome
Reversed	1
HGVS	NC_000002.11:g.215645400delT
CLNSRC
CLNACC	RCV000167393.1,