rs397508844

Orientation

minus

Stabilized

minus

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

Make rs397508844(-;-)

Reference

GRCh38 38.1/141

Chromosome

17

Position

43094353

Gene

BRCA1

is a	snp
is	mentioned by
dbSNP	rs397508844
dbSNP (classic)	rs397508844
ClinGen	rs397508844
ebi	rs397508844
HLI	rs397508844
Exac	rs397508844
Gnomad	rs397508844
Varsome	rs397508844
LitVar	rs397508844
Map	rs397508844
PheGenI	rs397508844
Biobank	rs397508844
1000 genomes	rs397508844
hgdp	rs397508844
ensembl	rs397508844
geneview	rs397508844
scholar	rs397508844
google	rs397508844
pharmgkb	rs397508844
gwascentral	rs397508844
openSNP	rs397508844
23andMe	rs397508844
SNPshot	rs397508844
SNPdbe	rs397508844
MSV3d	rs397508844
GWAS Ctlg	rs397508844

Max Magnitude

6

aka c.787+388_787+391del

ClinVar
Risk	rs397508844(-;-)
Alt	rs397508844(-;-)
Reference	Rs397508844(TGTT;TGTT)
Significance	Untested
Disease	Familial cancer of breast
Variation	info
Gene	BRCA1
CLNDBN	Familial cancer of breast
Reversed	1
HGVS	NC_000017.10:g.41246370_41246373delAACA
CLNSRC	ClinVar
CLNACC	RCV000047371.2,