rs397508855

Orientation

minus

Stabilized

minus

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

Make rs397508855(G;G)

Reference

GRCh38 38.1/141

Chromosome

17

Position

43094191

Gene

BRCA1

is a	snp
is	mentioned by
dbSNP	rs397508855
dbSNP (classic)	rs397508855
ClinGen	rs397508855
ebi	rs397508855
HLI	rs397508855
Exac	rs397508855
Gnomad	rs397508855
Varsome	rs397508855
LitVar	rs397508855
Map	rs397508855
PheGenI	rs397508855
Biobank	rs397508855
1000 genomes	rs397508855
hgdp	rs397508855
ensembl	rs397508855
geneview	rs397508855
scholar	rs397508855
google	rs397508855
pharmgkb	rs397508855
gwascentral	rs397508855
openSNP	rs397508855
23andMe	rs397508855
SNPshot	rs397508855
SNPdbe	rs397508855
MSV3d	rs397508855
GWAS Ctlg	rs397508855

Max Magnitude

6

aka c.787+552dup

ClinVar
Risk	rs397508855(G;G)
Alt	rs397508855(G;G)
Reference	Rs397508855(-;-)
Significance	Untested
Disease	Familial cancer of breast
Variation	info
Gene	BRCA1
CLNDBN	Familial cancer of breast
Reversed	1
HGVS	NC_000017.10:g.41246209dupC
CLNSRC	ClinVar
CLNACC	RCV000047424.2,