rs397509067

Orientation

minus

Stabilized

minus

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

Make rs397509067(-;-)

Reference

GRCh38 38.1/141

Chromosome

17

Position

43092092

Gene

BRCA1

is a	snp
is	mentioned by
dbSNP	rs397509067
dbSNP (classic)	rs397509067
ClinGen	rs397509067
ebi	rs397509067
HLI	rs397509067
Exac	rs397509067
Gnomad	rs397509067
Varsome	rs397509067
LitVar	rs397509067
Map	rs397509067
PheGenI	rs397509067
Biobank	rs397509067
1000 genomes	rs397509067
hgdp	rs397509067
ensembl	rs397509067
geneview	rs397509067
scholar	rs397509067
google	rs397509067
pharmgkb	rs397509067
gwascentral	rs397509067
openSNP	rs397509067
23andMe	rs397509067
SNPshot	rs397509067
SNPdbe	rs397509067
MSV3d	rs397509067
GWAS Ctlg	rs397509067

Max Magnitude

6

ClinVar
Risk	rs397509067(-;-)
Alt	rs397509067(-;-)
Reference	Rs397509067(TGTT;TGTT)
Significance	Pathogenic
Disease	Hereditary breast and ovarian cancer syndrome Breast-ovarian cancer not specified Familial cancer of breast not provided
Variation	info
Gene	BRCA1
CLNDBN	Hereditary breast and ovarian cancer syndrome Breast-ovarian cancer, familial 1 not specified Familial cancer of breast not provided
Reversed	1
HGVS	NC_000017.10:g.41244109_41244112delAACA
CLNSRC	ClinVar
CLNACC	RCV000048197.3, RCV000077549.4, RCV000239029.1, RCV000459696.1, RCV000478411.1,