rs397509337

Orientation

minus

Stabilized

minus

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

Make rs397509337(-;-)

Reference

GRCh38 38.1/141

Chromosome

17

Position

43094604

Gene

BRCA1

is a	snp
is	mentioned by
dbSNP	rs397509337
dbSNP (classic)	rs397509337
ClinGen	rs397509337
ebi	rs397509337
HLI	rs397509337
Exac	rs397509337
Gnomad	rs397509337
Varsome	rs397509337
LitVar	rs397509337
Map	rs397509337
PheGenI	rs397509337
Biobank	rs397509337
1000 genomes	rs397509337
hgdp	rs397509337
ensembl	rs397509337
geneview	rs397509337
scholar	rs397509337
google	rs397509337
pharmgkb	rs397509337
gwascentral	rs397509337
openSNP	rs397509337
23andMe	rs397509337
SNPshot	rs397509337
SNPdbe	rs397509337
MSV3d	rs397509337
GWAS Ctlg	rs397509337

Max Magnitude

6

ClinVar
Risk	rs397509337(-;-)
Alt	rs397509337(-;-)
Reference	Rs397509337(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.41246621delT
CLNSRC	ClinVar
CLNACC	RCV000049192.2, RCV000256934.2,