rs397508877

Orientation

minus

Stabilized

minus

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

Make rs397508877(T;T)

Reference

GRCh38 38.1/141

Chromosome

17

Position

43094018

Gene

BRCA1

is a	snp
is	mentioned by
dbSNP	rs397508877
dbSNP (classic)	rs397508877
ClinGen	rs397508877
ebi	rs397508877
HLI	rs397508877
Exac	rs397508877
Gnomad	rs397508877
Varsome	rs397508877
LitVar	rs397508877
Map	rs397508877
PheGenI	rs397508877
Biobank	rs397508877
1000 genomes	rs397508877
hgdp	rs397508877
ensembl	rs397508877
geneview	rs397508877
scholar	rs397508877
google	rs397508877
pharmgkb	rs397508877
gwascentral	rs397508877
openSNP	rs397508877
23andMe	rs397508877
SNPshot	rs397508877
SNPdbe	rs397508877
MSV3d	rs397508877
GWAS Ctlg	rs397508877

Max Magnitude

6

ClinVar
Risk	rs397508877(T;T)
Alt	rs397508877(T;T)
Reference	Rs397508877(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.41246035T>A
CLNSRC	ClinVar
CLNACC	RCV000047509.2, RCV000257326.2,