rs397509035

Orientation

minus

Stabilized

minus

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

Make rs397509035(G;G)

Reference

GRCh38 38.1/141

Chromosome

17

Position

43092409

Gene

BRCA1

is a	snp
is	mentioned by
dbSNP	rs397509035
dbSNP (classic)	rs397509035
ClinGen	rs397509035
ebi	rs397509035
HLI	rs397509035
Exac	rs397509035
Gnomad	rs397509035
Varsome	rs397509035
LitVar	rs397509035
Map	rs397509035
PheGenI	rs397509035
Biobank	rs397509035
1000 genomes	rs397509035
hgdp	rs397509035
ensembl	rs397509035
geneview	rs397509035
scholar	rs397509035
google	rs397509035
pharmgkb	rs397509035
gwascentral	rs397509035
openSNP	rs397509035
23andMe	rs397509035
SNPshot	rs397509035
SNPdbe	rs397509035
MSV3d	rs397509035
GWAS Ctlg	rs397509035

Max Magnitude

6

ClinVar
Risk	rs397509035(G;G)
Alt	rs397509035(G;G)
Reference	Rs397509035(C;C)
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.41244426G>C
CLNSRC	ClinVar
CLNACC	RCV000048075.2, RCV000256646.2,