rs786202919

Orientation

minus

Stabilized

minus

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

Make rs786202919(-;-)

Reference

GRCh38.p2 38.2/146

Chromosome

17

Position

43093123

Gene

BRCA1

is a	snp
is	mentioned by
dbSNP	rs786202919
dbSNP (classic)	rs786202919
ClinGen	rs786202919
ebi	rs786202919
HLI	rs786202919
Exac	rs786202919
Gnomad	rs786202919
Varsome	rs786202919
LitVar	rs786202919
Map	rs786202919
PheGenI	rs786202919
Biobank	rs786202919
1000 genomes	rs786202919
hgdp	rs786202919
ensembl	rs786202919
geneview	rs786202919
scholar	rs786202919
google	rs786202919
pharmgkb	rs786202919
gwascentral	rs786202919
openSNP	rs786202919
23andMe	rs786202919
SNPshot	rs786202919
SNPdbe	rs786202919
MSV3d	rs786202919
GWAS Ctlg	rs786202919

Max Magnitude

6

ClinVar
Risk	rs786202919(-;-)
Alt	rs786202919(-;-)
Reference	Rs786202919(AG;AG)
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.41245140_41245141delCT
CLNSRC
CLNACC	RCV000165987.1, RCV000241284.1,