rs878853296

Orientation

minus

Stabilized

minus

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

Make rs878853296(-;-)

Reference

GRCh38.p2 38.2/147

Chromosome

17

Position

43045771

Gene

BRCA1

is a	snp
is	mentioned by
dbSNP	rs878853296
dbSNP (classic)	rs878853296
ClinGen	rs878853296
ebi	rs878853296
HLI	rs878853296
Exac	rs878853296
Gnomad	rs878853296
Varsome	rs878853296
LitVar	rs878853296
Map	rs878853296
PheGenI	rs878853296
Biobank	rs878853296
1000 genomes	rs878853296
hgdp	rs878853296
ensembl	rs878853296
geneview	rs878853296
scholar	rs878853296
google	rs878853296
pharmgkb	rs878853296
gwascentral	rs878853296
openSNP	rs878853296
23andMe	rs878853296
SNPshot	rs878853296
SNPdbe	rs878853296
MSV3d	rs878853296
GWAS Ctlg	rs878853296

Max Magnitude

6

ClinVar
Risk	rs878853296(-;-)
Alt	rs878853296(-;-)
Reference	Rs878853296(GGTG;GGTG)
Significance	Pathogenic
Disease	Breast-ovarian cancer
Variation	info
Gene	BRCA1
CLNDBN	Breast-ovarian cancer, familial 1
Reversed	1
HGVS	NC_000017.10:g.41197788_41197791delCACC
CLNSRC
CLNACC	RCV000225437.2,