rs397508876

Orientation

minus

Stabilized

minus

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

Make rs397508876(-;-)

Reference

GRCh38 38.1/141

Chromosome

17

Position

43094021

Gene

BRCA1

is a	snp
is	mentioned by
dbSNP	rs397508876
dbSNP (classic)	rs397508876
ClinGen	rs397508876
ebi	rs397508876
HLI	rs397508876
Exac	rs397508876
Gnomad	rs397508876
Varsome	rs397508876
LitVar	rs397508876
Map	rs397508876
PheGenI	rs397508876
Biobank	rs397508876
1000 genomes	rs397508876
hgdp	rs397508876
ensembl	rs397508876
geneview	rs397508876
scholar	rs397508876
google	rs397508876
pharmgkb	rs397508876
gwascentral	rs397508876
openSNP	rs397508876
23andMe	rs397508876
SNPshot	rs397508876
SNPdbe	rs397508876
MSV3d	rs397508876
GWAS Ctlg	rs397508876

Max Magnitude

6

aka c.787+719_787+723del

ClinVar
Risk	rs397508876(-;-)
Alt	rs397508876(-;-)
Reference	Rs397508876(AAAGC;AAAGC)
Significance	Untested
Disease	Familial cancer of breast
Variation	info
Gene	BRCA1
CLNDBN	Familial cancer of breast
Reversed	1
HGVS	NC_000017.10:g.41246038_41246042delGCTTT
CLNSRC	ClinVar
CLNACC	RCV000047501.2,