rs397508905

Orientation

minus

Stabilized

minus

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

Make rs397508905(T;T)

Reference

GRCh38 38.1/141

Chromosome

17

Position

43093790

Gene

BRCA1

is a	snp
is	mentioned by
dbSNP	rs397508905
dbSNP (classic)	rs397508905
ClinGen	rs397508905
ebi	rs397508905
HLI	rs397508905
Exac	rs397508905
Gnomad	rs397508905
Varsome	rs397508905
LitVar	rs397508905
Map	rs397508905
PheGenI	rs397508905
Biobank	rs397508905
1000 genomes	rs397508905
hgdp	rs397508905
ensembl	rs397508905
geneview	rs397508905
scholar	rs397508905
google	rs397508905
pharmgkb	rs397508905
gwascentral	rs397508905
openSNP	rs397508905
23andMe	rs397508905
SNPshot	rs397508905
SNPdbe	rs397508905
MSV3d	rs397508905
GWAS Ctlg	rs397508905

Max Magnitude

6

ClinVar
Risk	rs397508905(T;T)
Alt	rs397508905(T;T)
Reference	Rs397508905(A;A)
Significance	Untested
Disease	Familial cancer of breast
Variation	info
Gene	BRCA1
CLNDBN	Familial cancer of breast
Reversed	1
HGVS	NC_000017.10:g.41245807T>A
CLNSRC	ClinVar
CLNACC	RCV000047574.2,