rs397509186

Orientation

minus

Stabilized

minus

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

Make rs397509186(-;-)

Reference

GRCh38 38.1/141

Chromosome

17

Position

43074341

Gene

BRCA1

is a	snp
is	mentioned by
dbSNP	rs397509186
dbSNP (classic)	rs397509186
ClinGen	rs397509186
ebi	rs397509186
HLI	rs397509186
Exac	rs397509186
Gnomad	rs397509186
Varsome	rs397509186
LitVar	rs397509186
Map	rs397509186
PheGenI	rs397509186
Biobank	rs397509186
1000 genomes	rs397509186
hgdp	rs397509186
ensembl	rs397509186
geneview	rs397509186
scholar	rs397509186
google	rs397509186
pharmgkb	rs397509186
gwascentral	rs397509186
openSNP	rs397509186
23andMe	rs397509186
SNPshot	rs397509186
SNPdbe	rs397509186
MSV3d	rs397509186
GWAS Ctlg	rs397509186

Max Magnitude

6

aka c.4646_4665del

ClinVar
Risk	rs397509186(-;-)
Alt	rs397509186(-;-)
Reference	Rs397509186(AAACATCTTACTTGCCAAGG;AAACATCTTACTTGCCAAGG)
Significance	Untested
Disease	Familial cancer of breast
Variation	info
Gene	BRCA1
CLNDBN	Familial cancer of breast
Reversed	1
HGVS	NC_000017.10:g.41226358_41226377del20
CLNSRC	ClinVar
CLNACC	RCV000048617.2,