rs587782666

Orientation

minus

Stabilized

minus

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

Make rs587782666(-;-)

Reference

GRCh38.p2 38.2/144

Chromosome

17

Position

43104225

Gene

BRCA1

is a	snp
is	mentioned by
dbSNP	rs587782666
dbSNP (classic)	rs587782666
ClinGen	rs587782666
ebi	rs587782666
HLI	rs587782666
Exac	rs587782666
Gnomad	rs587782666
Varsome	rs587782666
LitVar	rs587782666
Map	rs587782666
PheGenI	rs587782666
Biobank	rs587782666
1000 genomes	rs587782666
hgdp	rs587782666
ensembl	rs587782666
geneview	rs587782666
scholar	rs587782666
google	rs587782666
pharmgkb	rs587782666
gwascentral	rs587782666
openSNP	rs587782666
23andMe	rs587782666
SNPshot	rs587782666
SNPdbe	rs587782666
MSV3d	rs587782666
GWAS Ctlg	rs587782666

Max Magnitude

6

BRCA1, c.335_338delATAA (p.Asn112Thrfs)

ClinVar
Risk	rs587782666(-;-)
Alt	rs587782666(-;-)
Reference	Rs587782666(ATAA;ATAA)
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.41256242_41256245delTTAT
CLNSRC
CLNACC	RCV000132087.2, RCV000241264.1,