rs876658626

Orientation

minus

Stabilized

minus

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

Make rs876658626(-;-)

Reference

GRCh38.p2 38.2/147

Chromosome

17

Position

43092237

Gene

BRCA1

is a	snp
is	mentioned by
dbSNP	rs876658626
dbSNP (classic)	rs876658626
ClinGen	rs876658626
ebi	rs876658626
HLI	rs876658626
Exac	rs876658626
Gnomad	rs876658626
Varsome	rs876658626
LitVar	rs876658626
Map	rs876658626
PheGenI	rs876658626
Biobank	rs876658626
1000 genomes	rs876658626
hgdp	rs876658626
ensembl	rs876658626
geneview	rs876658626
scholar	rs876658626
google	rs876658626
pharmgkb	rs876658626
gwascentral	rs876658626
openSNP	rs876658626
23andMe	rs876658626
SNPshot	rs876658626
SNPdbe	rs876658626
MSV3d	rs876658626
GWAS Ctlg	rs876658626

Max Magnitude

6

aka c.788-1205del

ClinVar
Risk	rs876658626(-;-)
Alt	rs876658626(-;-)
Reference	Rs876658626(T;T)
Significance	Pathogenic
Disease	Hereditary cancer-predisposing syndrome
Variation	info
Gene	BRCA1
CLNDBN	Hereditary cancer-predisposing syndrome
Reversed	1
HGVS	NC_000017.10:g.41244254delA
CLNSRC
CLNACC	RCV000216850.1,