rs397509021

Orientation

minus

Stabilized

minus

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

Make rs397509021(-;-)

Reference

GRCh38 38.1/141

Chromosome

17

Position

43092655

Gene

BRCA1

is a	snp
is	mentioned by
dbSNP	rs397509021
dbSNP (classic)	rs397509021
ClinGen	rs397509021
ebi	rs397509021
HLI	rs397509021
Exac	rs397509021
Gnomad	rs397509021
Varsome	rs397509021
LitVar	rs397509021
Map	rs397509021
PheGenI	rs397509021
Biobank	rs397509021
1000 genomes	rs397509021
hgdp	rs397509021
ensembl	rs397509021
geneview	rs397509021
scholar	rs397509021
google	rs397509021
pharmgkb	rs397509021
gwascentral	rs397509021
openSNP	rs397509021
23andMe	rs397509021
SNPshot	rs397509021
SNPdbe	rs397509021
MSV3d	rs397509021
GWAS Ctlg	rs397509021

Max Magnitude

6

aka c.788-1627_788-1623del

ClinVar
Risk	rs397509021(-;-)
Alt	rs397509021(-;-)
Reference	Rs397509021(TTCAG;TTCAG)
Significance	Untested
Disease	Familial cancer of breast
Variation	info
Gene	BRCA1
CLNDBN	Familial cancer of breast
Reversed	1
HGVS	NC_000017.10:g.41244672_41244676delCTGAA
CLNSRC	ClinVar
CLNACC	RCV000047998.2,