rs397509097

Orientation

minus

Stabilized

minus

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

Make rs397509097(C;C)

Reference

GRCh38 38.1/141

Chromosome

17

Position

43091814

Gene

BRCA1

is a	snp
is	mentioned by
dbSNP	rs397509097
dbSNP (classic)	rs397509097
ClinGen	rs397509097
ebi	rs397509097
HLI	rs397509097
Exac	rs397509097
Gnomad	rs397509097
Varsome	rs397509097
LitVar	rs397509097
Map	rs397509097
PheGenI	rs397509097
Biobank	rs397509097
1000 genomes	rs397509097
hgdp	rs397509097
ensembl	rs397509097
geneview	rs397509097
scholar	rs397509097
google	rs397509097
pharmgkb	rs397509097
gwascentral	rs397509097
openSNP	rs397509097
23andMe	rs397509097
SNPshot	rs397509097
SNPdbe	rs397509097
MSV3d	rs397509097
GWAS Ctlg	rs397509097

Max Magnitude

6

aka c.788-783dup

ClinVar
Risk	rs397509097(C;C)
Alt	rs397509097(C;C)
Reference	Rs397509097(-;-)
Significance	Untested
Disease	Familial cancer of breast
Variation	info
Gene	BRCA1
CLNDBN	Familial cancer of breast
Reversed	1
HGVS	NC_000017.10:g.41243832dupG
CLNSRC	ClinVar
CLNACC	RCV000048300.2,