rs876658791

Orientation

minus

Stabilized

minus

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

Make rs876658791(-;-)

Reference

GRCh38.p2 38.2/147

Chromosome

17

Position

43093242

Gene

BRCA1

is a	snp
is	mentioned by
dbSNP	rs876658791
dbSNP (classic)	rs876658791
ClinGen	rs876658791
ebi	rs876658791
HLI	rs876658791
Exac	rs876658791
Gnomad	rs876658791
Varsome	rs876658791
LitVar	rs876658791
Map	rs876658791
PheGenI	rs876658791
Biobank	rs876658791
1000 genomes	rs876658791
hgdp	rs876658791
ensembl	rs876658791
geneview	rs876658791
scholar	rs876658791
google	rs876658791
pharmgkb	rs876658791
gwascentral	rs876658791
openSNP	rs876658791
23andMe	rs876658791
SNPshot	rs876658791
SNPdbe	rs876658791
MSV3d	rs876658791
GWAS Ctlg	rs876658791

Max Magnitude

6

aka c.787+1502del

ClinVar
Risk	rs876658791(-;-)
Alt	rs876658791(-;-)
Reference	Rs876658791(T;T)
Significance	Pathogenic
Disease	Hereditary cancer-predisposing syndrome
Variation	info
Gene	BRCA1
CLNDBN	Hereditary cancer-predisposing syndrome
Reversed	1
HGVS	NC_000017.10:g.41245259delA
CLNSRC
CLNACC	RCV000220988.1,