rs80358150

Orientation

minus

Stabilized

minus

Geno	Mag	Summary
(A;G)	6	BRCA1 variant considered pathogenic for breast cancer
(C;G)	6	BRCA1 variant considered pathogenic for breast cancer
(G;G)	0	Normal
(G;T)	6	BRCA1 variant considered pathogenic for breast cancer

Make rs80358150(A;A)

Reference

GRCh38 38.1/141

Chromosome

17

Position

43057051

Gene

BRCA1

is a	snp
is	mentioned by
dbSNP	rs80358150
dbSNP (classic)	rs80358150
ClinGen	rs80358150
ebi	rs80358150
HLI	rs80358150
Exac	rs80358150
Gnomad	rs80358150
Varsome	rs80358150
LitVar	rs80358150
Map	rs80358150
PheGenI	rs80358150
Biobank	rs80358150
1000 genomes	rs80358150
hgdp	rs80358150
ensembl	rs80358150
geneview	rs80358150
scholar	rs80358150
google	rs80358150
pharmgkb	rs80358150
gwascentral	rs80358150
openSNP	rs80358150
23andMe	rs80358150
SNPshot	rs80358150
SNPdbe	rs80358150
MSV3d	rs80358150
GWAS Ctlg	rs80358150

Max Magnitude

6

ClinVar
Risk	rs80358150(A;A) rs80358150(C;C)
Alt	rs80358150(A;A) rs80358150(C;C)
Reference	Rs80358150(G;G)
Significance	Pathogenic
Disease	Familial cancer of breast Breast-ovarian cancer Hereditary breast and ovarian cancer syndrome Hereditary cancer-predisposing syndrome not provided
Variation	info
Gene	BRCA1
CLNDBN	Familial cancer of breast Breast-ovarian cancer, familial 1 Hereditary breast and ovarian cancer syndrome Hereditary cancer-predisposing syndrome not provided
Reversed	1
HGVS	NC_000017.10:g.41209068C>G; NC_000017.10:g.41209068C>T
CLNSRC	Breast Cancer Information Core (BRCA1) Database of BRCA1 and BRCA2 sequence variants that have been clinically reclassified by a quantitative integrated evaluation
CLNACC	RCV000048897.2, RCV000031235.7, RCV000074601.6, RCV000131865.4, RCV000235135.2,