rs587780035

Orientation

minus

Stabilized

minus

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

Make rs587780035(C;G)

Make rs587780035(G;G)

Reference

GRCh38.p2 38.2/147

Chromosome

2

Position

214781165

Gene

BARD1

is a	snp
is	mentioned by
dbSNP	rs587780035
dbSNP (classic)	rs587780035
ClinGen	rs587780035
ebi	rs587780035
HLI	rs587780035
Exac	rs587780035
Gnomad	rs587780035
Varsome	rs587780035
LitVar	rs587780035
Map	rs587780035
PheGenI	rs587780035
Biobank	rs587780035
1000 genomes	rs587780035
hgdp	rs587780035
ensembl	rs587780035
geneview	rs587780035
scholar	rs587780035
google	rs587780035
pharmgkb	rs587780035
gwascentral	rs587780035
openSNP	rs587780035
23andMe	rs587780035
SNPshot	rs587780035
SNPdbe	rs587780035
MSV3d	rs587780035
GWAS Ctlg	rs587780035

Max Magnitude

0

ClinVar
Risk	rs587780035(G;G) rs587780035(T;T)
Alt	rs587780035(G;G) rs587780035(T;T)
Reference	Rs587780035(C;C)
Significance	Pathogenic
Disease	Hereditary cancer-predisposing syndrome not provided Familial cancer of breast not specified
Variation	info
Gene	BARD1
CLNDBN	Hereditary cancer-predisposing syndrome not provided Familial cancer of breast not specified
Reversed	1
HGVS	NC_000002.11:g.215645889G>A; NC_000002.11:g.215645889G>C
CLNSRC
CLNACC	RCV000221541.1, RCV000486426.1, RCV000115641.6, RCV000205761.2, RCV000212120.2,