rs397509314

Orientation

minus

Stabilized

minus

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

Make rs397509314(A;A)

Reference

GRCh38 38.1/141

Chromosome

17

Position

43094788

Gene

BRCA1

is a	snp
is	mentioned by
dbSNP	rs397509314
dbSNP (classic)	rs397509314
ClinGen	rs397509314
ebi	rs397509314
HLI	rs397509314
Exac	rs397509314
Gnomad	rs397509314
Varsome	rs397509314
LitVar	rs397509314
Map	rs397509314
PheGenI	rs397509314
Biobank	rs397509314
1000 genomes	rs397509314
hgdp	rs397509314
ensembl	rs397509314
geneview	rs397509314
scholar	rs397509314
google	rs397509314
pharmgkb	rs397509314
gwascentral	rs397509314
openSNP	rs397509314
23andMe	rs397509314
SNPshot	rs397509314
SNPdbe	rs397509314
MSV3d	rs397509314
GWAS Ctlg	rs397509314

Max Magnitude

6

aka c.742dup

ClinVar
Risk	rs397509314(A;A)
Alt	rs397509314(A;A)
Reference	Rs397509314(-;-)
Significance	Untested
Disease	Familial cancer of breast
Variation	info
Gene	BRCA1
CLNDBN	Familial cancer of breast
Reversed	1
HGVS	NC_000017.10:g.41246806dupT
CLNSRC	ClinVar
CLNACC	RCV000049117.2,