rs587781707

Orientation

minus

Stabilized

minus

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

Make rs587781707(C;G)

Make rs587781707(G;G)

Reference

GRCh38.p2 38.2/144

Chromosome

2

Position

214752472

Gene

BARD1

is a	snp
is	mentioned by
dbSNP	rs587781707
dbSNP (classic)	rs587781707
ClinGen	rs587781707
ebi	rs587781707
HLI	rs587781707
Exac	rs587781707
Gnomad	rs587781707
Varsome	rs587781707
LitVar	rs587781707
Map	rs587781707
PheGenI	rs587781707
Biobank	rs587781707
1000 genomes	rs587781707
hgdp	rs587781707
ensembl	rs587781707
geneview	rs587781707
scholar	rs587781707
google	rs587781707
pharmgkb	rs587781707
gwascentral	rs587781707
openSNP	rs587781707
23andMe	rs587781707
SNPshot	rs587781707
SNPdbe	rs587781707
MSV3d	rs587781707
GWAS Ctlg	rs587781707

Max Magnitude

0

ClinVar
Risk	rs587781707(G;G) rs587781707(T;T)
Alt	rs587781707(G;G) rs587781707(T;T)
Reference	Rs587781707(C;C)
Significance	Pathogenic
Disease	Familial cancer of breast not specified Hereditary cancer-predisposing syndrome not provided
Variation	info
Gene	BARD1
CLNDBN	Familial cancer of breast not specified Hereditary cancer-predisposing syndrome not provided
Reversed	1
HGVS	NC_000002.11:g.215617196G>A; NC_000002.11:g.215617196G>C
CLNSRC
CLNACC	RCV000205925.1, RCV000480294.1, RCV000129880.5, RCV000206283.3, RCV000212133.1,