rs786203884

Orientation

minus

Stabilized

minus

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

Make rs786203884(G;G)

Reference

GRCh38.p2 38.2/146

Chromosome

17

Position

43091905

Gene

BRCA1

is a	snp
is	mentioned by
dbSNP	rs786203884
dbSNP (classic)	rs786203884
ClinGen	rs786203884
ebi	rs786203884
HLI	rs786203884
Exac	rs786203884
Gnomad	rs786203884
Varsome	rs786203884
LitVar	rs786203884
Map	rs786203884
PheGenI	rs786203884
Biobank	rs786203884
1000 genomes	rs786203884
hgdp	rs786203884
ensembl	rs786203884
geneview	rs786203884
scholar	rs786203884
google	rs786203884
pharmgkb	rs786203884
gwascentral	rs786203884
openSNP	rs786203884
23andMe	rs786203884
SNPshot	rs786203884
SNPdbe	rs786203884
MSV3d	rs786203884
GWAS Ctlg	rs786203884

Max Magnitude

6

ClinVar
Risk	rs786203884(G;G)
Alt	rs786203884(G;G)
Reference	Rs786203884(T;T)
Significance	Pathogenic
Disease	Hereditary cancer-predisposing syndrome Breast-ovarian cancer
Variation	info
Gene	BRCA1
CLNDBN	Hereditary cancer-predisposing syndrome Breast-ovarian cancer, familial 1
Reversed	1
HGVS	NC_000017.10:g.41243922A>C
CLNSRC
CLNACC	RCV000167384.1, RCV000240983.2,