rs786202064

Orientation

minus

Stabilized

minus

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

Make rs786202064(T;T)

Reference

GRCh38.p2 38.2/146

Chromosome

17

Position

43071080

Gene

BRCA1

is a	snp
is	mentioned by
dbSNP	rs786202064
dbSNP (classic)	rs786202064
ClinGen	rs786202064
ebi	rs786202064
HLI	rs786202064
Exac	rs786202064
Gnomad	rs786202064
Varsome	rs786202064
LitVar	rs786202064
Map	rs786202064
PheGenI	rs786202064
Biobank	rs786202064
1000 genomes	rs786202064
hgdp	rs786202064
ensembl	rs786202064
geneview	rs786202064
scholar	rs786202064
google	rs786202064
pharmgkb	rs786202064
gwascentral	rs786202064
openSNP	rs786202064
23andMe	rs786202064
SNPshot	rs786202064
SNPdbe	rs786202064
MSV3d	rs786202064
GWAS Ctlg	rs786202064

Max Magnitude

6

ClinVar
Risk	rs786202064(T;T)
Alt	rs786202064(T;T)
Reference	Rs786202064(C;C)
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.41223097G>A
CLNSRC
CLNACC	RCV000164690.1, RCV000241386.2,