rs397508956

Orientation

minus

Stabilized

minus

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

Make rs397508956(-;-)

Reference

GRCh38 38.1/141

Chromosome

17

Position

43093223

Gene

BRCA1

is a	snp
is	mentioned by
dbSNP	rs397508956
dbSNP (classic)	rs397508956
ClinGen	rs397508956
ebi	rs397508956
HLI	rs397508956
Exac	rs397508956
Gnomad	rs397508956
Varsome	rs397508956
LitVar	rs397508956
Map	rs397508956
PheGenI	rs397508956
Biobank	rs397508956
1000 genomes	rs397508956
hgdp	rs397508956
ensembl	rs397508956
geneview	rs397508956
scholar	rs397508956
google	rs397508956
pharmgkb	rs397508956
gwascentral	rs397508956
openSNP	rs397508956
23andMe	rs397508956
SNPshot	rs397508956
SNPdbe	rs397508956
MSV3d	rs397508956
GWAS Ctlg	rs397508956

Max Magnitude

6

aka c.787+1521del

ClinVar
Risk	rs397508956(-;-)
Alt	rs397508956(-;-)
Reference	Rs397508956(T;T)
Significance	Untested
Disease	Familial cancer of breast
Variation	info
Gene	BRCA1
CLNDBN	Familial cancer of breast
Reversed	1
HGVS	NC_000017.10:g.41245240delA
CLNSRC	ClinVar
CLNACC	RCV000047790.2,