rs876659072

Orientation

minus

Stabilized

minus

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

Make rs876659072(-;-)

Reference

GRCh38.p2 38.2/147

Chromosome

17

Position

43092814

Gene

BRCA1

is a	snp
is	mentioned by
dbSNP	rs876659072
dbSNP (classic)	rs876659072
ClinGen	rs876659072
ebi	rs876659072
HLI	rs876659072
Exac	rs876659072
Gnomad	rs876659072
Varsome	rs876659072
LitVar	rs876659072
Map	rs876659072
PheGenI	rs876659072
Biobank	rs876659072
1000 genomes	rs876659072
hgdp	rs876659072
ensembl	rs876659072
geneview	rs876659072
scholar	rs876659072
google	rs876659072
pharmgkb	rs876659072
gwascentral	rs876659072
openSNP	rs876659072
23andMe	rs876659072
SNPshot	rs876659072
SNPdbe	rs876659072
MSV3d	rs876659072
GWAS Ctlg	rs876659072

Max Magnitude

6

aka c.788-1782del

ClinVar
Risk	rs876659072(-;-)
Alt	rs876659072(-;-)
Reference	Rs876659072(A;A)
Significance	Pathogenic
Disease	Hereditary cancer-predisposing syndrome
Variation	info
Gene	BRCA1
CLNDBN	Hereditary cancer-predisposing syndrome
Reversed	1
HGVS	NC_000017.10:g.41244831delT
CLNSRC
CLNACC	RCV000219226.1,