rs876660305

Orientation

minus

Stabilized

minus

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

Make rs876660305(AC;T)

Make rs876660305(T;T)

Reference

GRCh38.p2 38.2/147

Chromosome

17

Position

43093144

Gene

BRCA1

is a	snp
is	mentioned by
dbSNP	rs876660305
dbSNP (classic)	rs876660305
ClinGen	rs876660305
ebi	rs876660305
HLI	rs876660305
Exac	rs876660305
Gnomad	rs876660305
Varsome	rs876660305
LitVar	rs876660305
Map	rs876660305
PheGenI	rs876660305
Biobank	rs876660305
1000 genomes	rs876660305
hgdp	rs876660305
ensembl	rs876660305
geneview	rs876660305
scholar	rs876660305
google	rs876660305
pharmgkb	rs876660305
gwascentral	rs876660305
openSNP	rs876660305
23andMe	rs876660305
SNPshot	rs876660305
SNPdbe	rs876660305
MSV3d	rs876660305
GWAS Ctlg	rs876660305

Max Magnitude

6

ClinVar
Risk	rs876660305(T;T)
Alt	rs876660305(T;T)
Reference	Rs876660305(AC;AC)
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.41245161_41245162delGTinsA
CLNSRC
CLNACC	RCV000221355.1, RCV000257548.2,