rs397508839

Orientation

minus

Stabilized

minus

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

Make rs397508839(-;-)

Reference

GRCh38 38.1/141

Chromosome

17

Position

43094408

Gene

BRCA1

is a	snp
is	mentioned by
dbSNP	rs397508839
dbSNP (classic)	rs397508839
ClinGen	rs397508839
ebi	rs397508839
HLI	rs397508839
Exac	rs397508839
Gnomad	rs397508839
Varsome	rs397508839
LitVar	rs397508839
Map	rs397508839
PheGenI	rs397508839
Biobank	rs397508839
1000 genomes	rs397508839
hgdp	rs397508839
ensembl	rs397508839
geneview	rs397508839
scholar	rs397508839
google	rs397508839
pharmgkb	rs397508839
gwascentral	rs397508839
openSNP	rs397508839
23andMe	rs397508839
SNPshot	rs397508839
SNPdbe	rs397508839
MSV3d	rs397508839
GWAS Ctlg	rs397508839

Max Magnitude

6

aka c.787+335_787+336del

ClinVar
Risk	rs397508839(-;-)
Alt	rs397508839(-;-)
Reference	Rs397508839(AC;AC)
Significance	Untested
Disease	Familial cancer of breast
Variation	info
Gene	BRCA1
CLNDBN	Familial cancer of breast
Reversed	1
HGVS	NC_000017.10:g.41246425_41246426delGT
CLNSRC	ClinVar
CLNACC	RCV000047352.2,