rs878853293

Orientation

minus

Stabilized

minus

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

Make rs878853293(-;-)

Reference

GRCh38.p2 38.2/147

Chromosome

17

Position

43074436

Gene

BRCA1

is a	snp
is	mentioned by
dbSNP	rs878853293
dbSNP (classic)	rs878853293
ClinGen	rs878853293
ebi	rs878853293
HLI	rs878853293
Exac	rs878853293
Gnomad	rs878853293
Varsome	rs878853293
LitVar	rs878853293
Map	rs878853293
PheGenI	rs878853293
Biobank	rs878853293
1000 genomes	rs878853293
hgdp	rs878853293
ensembl	rs878853293
geneview	rs878853293
scholar	rs878853293
google	rs878853293
pharmgkb	rs878853293
gwascentral	rs878853293
openSNP	rs878853293
23andMe	rs878853293
SNPshot	rs878853293
SNPdbe	rs878853293
MSV3d	rs878853293
GWAS Ctlg	rs878853293

Max Magnitude

6

ClinVar
Risk	rs878853293(-;-)
Alt	rs878853293(-;-)
Reference	Rs878853293(T;T)
Significance	Pathogenic
Disease	Breast-ovarian cancer
Variation	info
Gene	BRCA1
CLNDBN	Breast-ovarian cancer, familial 1
Reversed	1
HGVS	NC_000017.10:g.41226453delA
CLNSRC
CLNACC	RCV000225462.2,