rs876659591

Orientation

minus

Stabilized

minus

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

Make rs876659591(CG;CG)

Reference

GRCh38.p2 38.2/147

Chromosome

17

Position

43093981

Gene

BRCA1

is a	snp
is	mentioned by
dbSNP	rs876659591
dbSNP (classic)	rs876659591
ClinGen	rs876659591
ebi	rs876659591
HLI	rs876659591
Exac	rs876659591
Gnomad	rs876659591
Varsome	rs876659591
LitVar	rs876659591
Map	rs876659591
PheGenI	rs876659591
Biobank	rs876659591
1000 genomes	rs876659591
hgdp	rs876659591
ensembl	rs876659591
geneview	rs876659591
scholar	rs876659591
google	rs876659591
pharmgkb	rs876659591
gwascentral	rs876659591
openSNP	rs876659591
23andMe	rs876659591
SNPshot	rs876659591
SNPdbe	rs876659591
MSV3d	rs876659591
GWAS Ctlg	rs876659591

Max Magnitude

6

aka c.787+755_787+763delinsCG

ClinVar
Risk	rs876659591(CG;CG)
Alt	rs876659591(CG;CG)
Reference	Rs876659591(TGAGGATTT;TGAGGATTT)
Significance	Pathogenic
Disease	Hereditary cancer-predisposing syndrome
Variation	info
Gene	BRCA1
CLNDBN	Hereditary cancer-predisposing syndrome
Reversed	1
HGVS	NC_000017.10:g.41245998_41246006delAAATCCTCAinsCG
CLNSRC
CLNACC	RCV000217286.1,