rs587776480

Orientation

plus

Stabilized

plus

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

Make rs587776480(-;-)

Reference

GRCh38 38.1/142

Chromosome

17

Position

43093915

Gene

BRCA1

is a	snp
is	mentioned by
dbSNP	rs587776480
dbSNP (classic)	rs587776480
ClinGen	rs587776480
ebi	rs587776480
HLI	rs587776480
Exac	rs587776480
Gnomad	rs587776480
Varsome	rs587776480
LitVar	rs587776480
Map	rs587776480
PheGenI	rs587776480
Biobank	rs587776480
1000 genomes	rs587776480
hgdp	rs587776480
ensembl	rs587776480
geneview	rs587776480
scholar	rs587776480
google	rs587776480
pharmgkb	rs587776480
gwascentral	rs587776480
openSNP	rs587776480
23andMe	rs587776480
SNPshot	rs587776480
SNPdbe	rs587776480
MSV3d	rs587776480
GWAS Ctlg	rs587776480

Max Magnitude

6

ClinVar
Risk	rs587776480(-;-)
Alt	rs587776480(-;-)
Reference	Rs587776480(GTTTG;GTTTG)
Significance	Pathogenic
Disease	Breast-ovarian cancer
Variation	info
Gene	BRCA1
CLNDBN	Breast-ovarian cancer, familial 1
Reversed	0
HGVS	NC_000017.10:g.41245932_41245936delGTTTG
CLNSRC	ClinVar
CLNACC	RCV000144201.2,