rs876659293

Orientation

minus

Stabilized

minus

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

Make rs876659293(-;-)

Reference

GRCh38.p2 38.2/147

Chromosome

17

Position

43074333

Gene

BRCA1

is a	snp
is	mentioned by
dbSNP	rs876659293
dbSNP (classic)	rs876659293
ClinGen	rs876659293
ebi	rs876659293
HLI	rs876659293
Exac	rs876659293
Gnomad	rs876659293
Varsome	rs876659293
LitVar	rs876659293
Map	rs876659293
PheGenI	rs876659293
Biobank	rs876659293
1000 genomes	rs876659293
hgdp	rs876659293
ensembl	rs876659293
geneview	rs876659293
scholar	rs876659293
google	rs876659293
pharmgkb	rs876659293
gwascentral	rs876659293
openSNP	rs876659293
23andMe	rs876659293
SNPshot	rs876659293
SNPdbe	rs876659293
MSV3d	rs876659293
GWAS Ctlg	rs876659293

Max Magnitude

6

aka c.4654_4673del

ClinVar
Risk	rs876659293(-;-)
Alt	rs876659293(-;-)
Reference	Rs876659293(TACTTGCCAAGGCAAGATCT;TACTTGCCAAGGCAAGATCT)
Significance	Pathogenic
Disease	Hereditary cancer-predisposing syndrome
Variation	info
Gene	BRCA1
CLNDBN	Hereditary cancer-predisposing syndrome
Reversed	1
HGVS	NC_000017.10:g.41226350_41226369del20
CLNSRC
CLNACC	RCV000217564.1,