rs397508968

Orientation

minus

Stabilized

minus

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

Make rs397508968(T;T)

Reference

GRCh38 38.1/141

Chromosome

17

Position

43093097

Gene

BRCA1

is a	snp
is	mentioned by
dbSNP	rs397508968
dbSNP (classic)	rs397508968
ClinGen	rs397508968
ebi	rs397508968
HLI	rs397508968
Exac	rs397508968
Gnomad	rs397508968
Varsome	rs397508968
LitVar	rs397508968
Map	rs397508968
PheGenI	rs397508968
Biobank	rs397508968
1000 genomes	rs397508968
hgdp	rs397508968
ensembl	rs397508968
geneview	rs397508968
scholar	rs397508968
google	rs397508968
pharmgkb	rs397508968
gwascentral	rs397508968
openSNP	rs397508968
23andMe	rs397508968
SNPshot	rs397508968
SNPdbe	rs397508968
MSV3d	rs397508968
GWAS Ctlg	rs397508968

Max Magnitude

6

ClinVar
Risk	rs397508968(T;T)
Alt	rs397508968(T;T)
Reference	Rs397508968(A;A)
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.41245114T>A
CLNSRC	ClinVar
CLNACC	RCV000047839.2, RCV000256965.2,