rs80357698

minus

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

Make rs80357698(-;-)

Reference

GRCh38 38.1/141

Chromosome

17

Position

43093920

Gene

BRCA1

is a	snp
is	mentioned by
dbSNP	rs80357698
dbSNP (classic)	rs80357698
ClinGen	rs80357698
ebi	rs80357698
HLI	rs80357698
Exac	rs80357698
Gnomad	rs80357698
Varsome	rs80357698
LitVar	rs80357698
Map	rs80357698
PheGenI	rs80357698
Biobank	rs80357698
1000 genomes	rs80357698
hgdp	rs80357698
ensembl	rs80357698
geneview	rs80357698
scholar	rs80357698
google	rs80357698
pharmgkb	rs80357698
gwascentral	rs80357698
openSNP	rs80357698
23andMe	rs80357698
SNPshot	rs80357698
SNPdbe	rs80357698
MSV3d	rs80357698
GWAS Ctlg	rs80357698

Max Magnitude

6

rs80357698, also known as 1727del4, c.1608_1611delTAAC and p.Thr536_Asn537?fs, is a variant in the BRCA1 gene considered pathogenic for breast cancer in ClinVar.

ClinVar
Risk	rs80357698(-;-)
Alt	rs80357698(-;-)
Reference	Rs80357698(TAAC;TAAC)
Significance	Pathogenic
Disease	Familial cancer of breast Breast-ovarian cancer
Variation	info
Gene	BRCA1
CLNDBN	Familial cancer of breast Breast-ovarian cancer, familial 1
Reversed	1
HGVS	NC_000017.10:g.41245937_41245940delGTTA
CLNSRC	Breast Cancer Information Core (BRCA1)
CLNACC	RCV000047538.2, RCV000111653.3,