rs786203811

Orientation

minus

Stabilized

minus

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

Make rs786203811(-;-)

Make rs786203811(-;CA)

Reference

GRCh38.p2 38.2/146

Chromosome

2

Position

214728861

Gene

BARD1

is a	snp
is	mentioned by
dbSNP	rs786203811
dbSNP (classic)	rs786203811
ClinGen	rs786203811
ebi	rs786203811
HLI	rs786203811
Exac	rs786203811
Gnomad	rs786203811
Varsome	rs786203811
LitVar	rs786203811
Map	rs786203811
PheGenI	rs786203811
Biobank	rs786203811
1000 genomes	rs786203811
hgdp	rs786203811
ensembl	rs786203811
geneview	rs786203811
scholar	rs786203811
google	rs786203811
pharmgkb	rs786203811
gwascentral	rs786203811
openSNP	rs786203811
23andMe	rs786203811
SNPshot	rs786203811
SNPdbe	rs786203811
MSV3d	rs786203811
GWAS Ctlg	rs786203811

Max Magnitude

0

ClinVar
Risk	rs786203811(-;-)
Alt	rs786203811(-;-)
Reference	Rs786203811(CA;CA)
Significance	Pathogenic
Disease	Hereditary cancer-predisposing syndrome
Variation	info
Gene	BARD1
CLNDBN	Hereditary cancer-predisposing syndrome
Reversed	1
HGVS	NC_000002.11:g.215593585_215593586delTG
CLNSRC
CLNACC	RCV000167280.1,