rs876659139

Orientation

minus

Stabilized

minus

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

Make rs876659139(-;-)

Reference

GRCh38.p2 38.2/147

Chromosome

17

Position

43094022

Gene

BRCA1

is a	snp
is	mentioned by
dbSNP	rs876659139
dbSNP (classic)	rs876659139
ClinGen	rs876659139
ebi	rs876659139
HLI	rs876659139
Exac	rs876659139
Gnomad	rs876659139
Varsome	rs876659139
LitVar	rs876659139
Map	rs876659139
PheGenI	rs876659139
Biobank	rs876659139
1000 genomes	rs876659139
hgdp	rs876659139
ensembl	rs876659139
geneview	rs876659139
scholar	rs876659139
google	rs876659139
pharmgkb	rs876659139
gwascentral	rs876659139
openSNP	rs876659139
23andMe	rs876659139
SNPshot	rs876659139
SNPdbe	rs876659139
MSV3d	rs876659139
GWAS Ctlg	rs876659139

Max Magnitude

6

ClinVar
Risk	rs876659139(-;-)
Alt	rs876659139(-;-)
Reference	Rs876659139(TAAAG;TAAAG)
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.41246039_41246043delCTTTA
CLNSRC
CLNACC	RCV000218408.1, RCV000256672.2,