rs397508951

Orientation

minus

Stabilized

minus

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

Make rs397508951(-;-)

Reference

GRCh38 38.1/141

Chromosome

17

Position

43093316

Gene

BRCA1

is a	snp
is	mentioned by
dbSNP	rs397508951
dbSNP (classic)	rs397508951
ClinGen	rs397508951
ebi	rs397508951
HLI	rs397508951
Exac	rs397508951
Gnomad	rs397508951
Varsome	rs397508951
LitVar	rs397508951
Map	rs397508951
PheGenI	rs397508951
Biobank	rs397508951
1000 genomes	rs397508951
hgdp	rs397508951
ensembl	rs397508951
geneview	rs397508951
scholar	rs397508951
google	rs397508951
pharmgkb	rs397508951
gwascentral	rs397508951
openSNP	rs397508951
23andMe	rs397508951
SNPshot	rs397508951
SNPdbe	rs397508951
MSV3d	rs397508951
GWAS Ctlg	rs397508951

Max Magnitude

6

ClinVar
Risk	rs397508951(-;-)
Alt	rs397508951(-;-)
Reference	Rs397508951(GTTA;GTTA)
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.41245333_41245336delTAAC
CLNSRC	ClinVar
CLNACC	RCV000047762.2, RCV000257649.2,