rs397508837

Orientation

minus

Stabilized

minus

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

Make rs397508837(-;-)

Reference

GRCh38 38.1/141

Chromosome

17

Position

43094419

Gene

BRCA1

is a	snp
is	mentioned by
dbSNP	rs397508837
dbSNP (classic)	rs397508837
ClinGen	rs397508837
ebi	rs397508837
HLI	rs397508837
Exac	rs397508837
Gnomad	rs397508837
Varsome	rs397508837
LitVar	rs397508837
Map	rs397508837
PheGenI	rs397508837
Biobank	rs397508837
1000 genomes	rs397508837
hgdp	rs397508837
ensembl	rs397508837
geneview	rs397508837
scholar	rs397508837
google	rs397508837
pharmgkb	rs397508837
gwascentral	rs397508837
openSNP	rs397508837
23andMe	rs397508837
SNPshot	rs397508837
SNPdbe	rs397508837
MSV3d	rs397508837
GWAS Ctlg	rs397508837

Max Magnitude

6

aka c.787+325del

ClinVar
Risk	rs397508837(-;-)
Alt	rs397508837(-;-)
Reference	Rs397508837(C;C)
Significance	Untested
Disease	Familial cancer of breast
Variation	info
Gene	BRCA1
CLNDBN	Familial cancer of breast
Reversed	1
HGVS	NC_000017.10:g.41246436delG
CLNSRC	ClinVar
CLNACC	RCV000047346.2,