rs80357107

Orientation

minus

Stabilized

minus

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

Make rs80357107(A;A)

Reference

GRCh38 38.1/141

Chromosome

17

Position

43045757

Gene

BRCA1

is a	snp
is	mentioned by
dbSNP	rs80357107
dbSNP (classic)	rs80357107
ClinGen	rs80357107
ebi	rs80357107
HLI	rs80357107
Exac	rs80357107
Gnomad	rs80357107
Varsome	rs80357107
LitVar	rs80357107
Map	rs80357107
PheGenI	rs80357107
Biobank	rs80357107
1000 genomes	rs80357107
hgdp	rs80357107
ensembl	rs80357107
geneview	rs80357107
scholar	rs80357107
google	rs80357107
pharmgkb	rs80357107
gwascentral	rs80357107
openSNP	rs80357107
23andMe	rs80357107
SNPshot	rs80357107
SNPdbe	rs80357107
MSV3d	rs80357107
GWAS Ctlg	rs80357107

Max Magnitude

6

ClinVar
Risk	rs80357107(A;A) rs80357107(G;G)
Alt	rs80357107(A;A) rs80357107(G;G)
Reference	Rs80357107(T;T)
Significance	Other
Disease	Breast-ovarian cancer Familial cancer of breast not provided
Variation	info
Gene	BRCA1
CLNDBN	Breast-ovarian cancer, familial 1 Familial cancer of breast not provided
Reversed	1
HGVS	NC_000017.10:g.41197774A>C; NC_000017.10:g.41197774A>T
CLNSRC	Database of BRCA1 and BRCA2 sequence variants that have been clinically reclassified by a quantitative integrated evaluation
CLNACC	RCV000241502.1, RCV000049032.2, RCV000077628.4, RCV000480633.1,