rs397508878

Orientation

minus

Stabilized

minus

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

Make rs397508878(T;T)

Reference

GRCh38 38.1/141

Chromosome

17

Position

43094017

Gene

BRCA1

is a	snp
is	mentioned by
dbSNP	rs397508878
dbSNP (classic)	rs397508878
ClinGen	rs397508878
ebi	rs397508878
HLI	rs397508878
Exac	rs397508878
Gnomad	rs397508878
Varsome	rs397508878
LitVar	rs397508878
Map	rs397508878
PheGenI	rs397508878
Biobank	rs397508878
1000 genomes	rs397508878
hgdp	rs397508878
ensembl	rs397508878
geneview	rs397508878
scholar	rs397508878
google	rs397508878
pharmgkb	rs397508878
gwascentral	rs397508878
openSNP	rs397508878
23andMe	rs397508878
SNPshot	rs397508878
SNPdbe	rs397508878
MSV3d	rs397508878
GWAS Ctlg	rs397508878

Max Magnitude

6

ClinVar
Risk	rs397508878(T;T)
Alt	rs397508878(T;T)
Reference	Rs397508878(-;-)
Significance	Pathogenic
Disease	Familial cancer of breast Breast-ovarian cancer
Variation	info
Gene	BRCA1
CLNDBN	Familial cancer of breast Breast-ovarian cancer, familial 1
Reversed	1
HGVS	NC_000017.10:g.41246034_41246035insA
CLNSRC	ClinVar
CLNACC	RCV000047510.2, RCV000257015.2,