rs80357837

minus

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

Make rs80357837(-;-)

Reference

GRCh38 38.1/141

Chromosome

17

Position

43071159

Gene

BRCA1

is a	snp
is	mentioned by
dbSNP	rs80357837
dbSNP (classic)	rs80357837
ClinGen	rs80357837
ebi	rs80357837
HLI	rs80357837
Exac	rs80357837
Gnomad	rs80357837
Varsome	rs80357837
LitVar	rs80357837
Map	rs80357837
PheGenI	rs80357837
Biobank	rs80357837
1000 genomes	rs80357837
hgdp	rs80357837
ensembl	rs80357837
geneview	rs80357837
scholar	rs80357837
google	rs80357837
pharmgkb	rs80357837
gwascentral	rs80357837
openSNP	rs80357837
23andMe	rs80357837
SNPshot	rs80357837
SNPdbe	rs80357837
MSV3d	rs80357837
GWAS Ctlg	rs80357837

Max Magnitude

6

rs80357837, also known as 4873delCA, c.4754_4755delCA and p.Pro1585Argfs, is a variant in the BRCA1 gene considered pathogenic for breast cancer in ClinVar.

ClinVar
Risk	rs80357837(-;-)
Alt	rs80357837(-;-)
Reference	Rs80357837(CA;CA)
Significance	Pathogenic
Disease	Familial cancer of breast Breast-ovarian cancer Hereditary cancer-predisposing syndrome not provided
Variation	info
Gene	BRCA1
CLNDBN	Familial cancer of breast Breast-ovarian cancer, familial 1 Hereditary cancer-predisposing syndrome not provided
Reversed	1
HGVS	NC_000017.10:g.41223176_41223177delTG
CLNSRC	Breast Cancer Information Core (BRCA1)
CLNACC	RCV000048652.2, RCV000112394.4, RCV000219878.1, RCV000483332.1,