rs80357442

Orientation

minus

Stabilized

minus

Geno	Mag	Summary
(G;G)	0	common in clinvar

Make rs80357442(C;C)

Make rs80357442(C;G)

Reference

GRCh38 38.1/141

Chromosome

17

Position

43057077

Gene

BRCA1

is a	snp
is	mentioned by
dbSNP	rs80357442
dbSNP (classic)	rs80357442
ClinGen	rs80357442
ebi	rs80357442
HLI	rs80357442
Exac	rs80357442
Gnomad	rs80357442
Varsome	rs80357442
LitVar	rs80357442
Map	rs80357442
PheGenI	rs80357442
Biobank	rs80357442
1000 genomes	rs80357442
hgdp	rs80357442
ensembl	rs80357442
geneview	rs80357442
scholar	rs80357442
google	rs80357442
pharmgkb	rs80357442
gwascentral	rs80357442
openSNP	rs80357442
23andMe	rs80357442
SNPshot	rs80357442
SNPdbe	rs80357442
MSV3d	rs80357442
GWAS Ctlg	rs80357442

Max Magnitude

0

ClinVar
Risk	rs80357442(A;A) rs80357442(C;C)
Alt	rs80357442(A;A) rs80357442(C;C)
Reference	Rs80357442(G;G)
Significance	Other
Disease	Familial cancer of breast Breast-ovarian cancer Breast and/or ovarian cancer Hereditary cancer-predisposing syndrome not specified Hereditary breast and ovarian cancer syndrome
Variation	info
Gene	BRCA1
CLNDBN	Familial cancer of breast Breast-ovarian cancer, familial 1 Breast and/or ovarian cancer Hereditary cancer-predisposing syndrome not specified Hereditary breast and ovarian cancer syndrome
Reversed	1
HGVS	NC_000017.10:g.41209094C>G; NC_000017.10:g.41209094C>T
CLNSRC	Database of BRCA1 and BRCA2 sequence variants that have been clinically reclassified by a quantitative integrated evaluation
CLNACC	RCV000048884.2, RCV000112580.1, RCV000112579.2, RCV000148392.1, RCV000162992.1, RCV000168520.3, RCV000257892.3,