rs587781825

Orientation

minus

Stabilized

minus

Geno	Mag	Summary
(-;GC)	6	BRCA1 variant considered pathogenic for breast cancer
(GC;GC)	0	common in clinvar

Make rs587781825(-;-)

Reference

GRCh38.p2 38.2/144

Chromosome

17

Position

43051084

Gene

BRCA1

is a	snp
is	mentioned by
dbSNP	rs587781825
dbSNP (classic)	rs587781825
ClinGen	rs587781825
ebi	rs587781825
HLI	rs587781825
Exac	rs587781825
Gnomad	rs587781825
Varsome	rs587781825
LitVar	rs587781825
Map	rs587781825
PheGenI	rs587781825
Biobank	rs587781825
1000 genomes	rs587781825
hgdp	rs587781825
ensembl	rs587781825
geneview	rs587781825
scholar	rs587781825
google	rs587781825
pharmgkb	rs587781825
gwascentral	rs587781825
openSNP	rs587781825
23andMe	rs587781825
SNPshot	rs587781825
SNPdbe	rs587781825
MSV3d	rs587781825
GWAS Ctlg	rs587781825

Max Magnitude

6

ClinVar
Risk	rs587781825(-;-)
Alt	rs587781825(-;-)
Reference	Rs587781825(GC;GC)
Significance	Pathogenic
Disease	Hereditary cancer-predisposing syndrome Breast-ovarian cancer
Variation	info
Gene	BRCA1
CLNDBN	Hereditary cancer-predisposing syndrome Breast-ovarian cancer, familial 1
Reversed	1
HGVS	NC_000017.10:g.41203101_41203102delGC
CLNSRC
CLNACC	RCV000130106.3, RCV000241300.1,