rs397509161

Orientation

minus

Stabilized

minus

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

Make rs397509161(-;-)

Reference

GRCh38 38.1/141

Chromosome

17

Position

43082453

Gene

BRCA1

is a	snp
is	mentioned by
dbSNP	rs397509161
dbSNP (classic)	rs397509161
ClinGen	rs397509161
ebi	rs397509161
HLI	rs397509161
Exac	rs397509161
Gnomad	rs397509161
Varsome	rs397509161
LitVar	rs397509161
Map	rs397509161
PheGenI	rs397509161
Biobank	rs397509161
1000 genomes	rs397509161
hgdp	rs397509161
ensembl	rs397509161
geneview	rs397509161
scholar	rs397509161
google	rs397509161
pharmgkb	rs397509161
gwascentral	rs397509161
openSNP	rs397509161
23andMe	rs397509161
SNPshot	rs397509161
SNPdbe	rs397509161
MSV3d	rs397509161
GWAS Ctlg	rs397509161

Max Magnitude

6

aka c.4164_4165delCT

ClinVar
Risk	rs397509161(-;-)
Alt	rs397509161(-;-)
Reference	Rs397509161(CT;CT)
Significance	Untested
Disease	Familial cancer of breast
Variation	info
Gene	BRCA1
CLNDBN	Familial cancer of breast
Reversed	1
HGVS	NC_000017.10:g.41234470_41234471delAG
CLNSRC	ClinVar
CLNACC	RCV000048518.2,