rs397509164

Orientation

minus

Stabilized

minus

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

Make rs397509164(AGAA;AGAA)

Reference

GRCh38 38.1/141

Chromosome

17

Position

43082422

Gene

BRCA1

is a	snp
is	mentioned by
dbSNP	rs397509164
dbSNP (classic)	rs397509164
ClinGen	rs397509164
ebi	rs397509164
HLI	rs397509164
Exac	rs397509164
Gnomad	rs397509164
Varsome	rs397509164
LitVar	rs397509164
Map	rs397509164
PheGenI	rs397509164
Biobank	rs397509164
1000 genomes	rs397509164
hgdp	rs397509164
ensembl	rs397509164
geneview	rs397509164
scholar	rs397509164
google	rs397509164
pharmgkb	rs397509164
gwascentral	rs397509164
openSNP	rs397509164
23andMe	rs397509164
SNPshot	rs397509164
SNPdbe	rs397509164
MSV3d	rs397509164
GWAS Ctlg	rs397509164

Max Magnitude

6

ClinVar
Risk	rs397509164(AGAA;AGAA)
Alt	rs397509164(AGAA;AGAA)
Reference	Rs397509164(;)
Significance	Untested
Disease	Familial cancer of breast
Variation	info
Gene	BRCA1
CLNDBN	Familial cancer of breast
Reversed	1
HGVS	NC_000017.10:g.41234440_41234443dupTTCT
CLNSRC
CLNACC	RCV000048527.2,