rs779427628

Orientation

plus

Stabilized

plus

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

Make rs779427628(-;-)

Make rs779427628(-;AT)

Reference

GRCh38.p2 38.2/144

Chromosome

2

Position

214781334

Gene

BARD1

is a	snp
is	mentioned by
dbSNP	rs779427628
dbSNP (classic)	rs779427628
ClinGen	rs779427628
ebi	rs779427628
HLI	rs779427628
Exac	rs779427628
Gnomad	rs779427628
Varsome	rs779427628
LitVar	rs779427628
Map	rs779427628
PheGenI	rs779427628
Biobank	rs779427628
1000 genomes	rs779427628
hgdp	rs779427628
ensembl	rs779427628
geneview	rs779427628
scholar	rs779427628
google	rs779427628
pharmgkb	rs779427628
gwascentral	rs779427628
openSNP	rs779427628
23andMe	rs779427628
SNPshot	rs779427628
SNPdbe	rs779427628
MSV3d	rs779427628
GWAS Ctlg	rs779427628

Max Magnitude

0

ClinVar
Risk	rs779427628(-;-)
Alt	rs779427628(-;-)
Reference	Rs779427628(AT;AT)
Significance	Pathogenic
Disease	Hereditary cancer-predisposing syndrome Familial cancer of breast not provided
Variation	info
Gene	BARD1
CLNDBN	Hereditary cancer-predisposing syndrome Familial cancer of breast not provided
Reversed	0
HGVS	NC_000002.11:g.215646058_215646059delAT
CLNSRC
CLNACC	RCV000166193.1, RCV000464643.1, RCV000487275.1,