rs80359537

plus

Geno	Mag	Summary
(-;TA)	6	BRCA2 variant considered pathogenic for breast cancer
(AT;AT)	0	common in clinvar
(TA;TA)	0	common in clinvar

Make rs80359537(-;-)

Reference

GRCh38 38.1/141

Chromosome

13

Position

32340151

Gene

BRCA2

is a	snp
is	mentioned by
dbSNP	rs80359537
dbSNP (classic)	rs80359537
ClinGen	rs80359537
ebi	rs80359537
HLI	rs80359537
Exac	rs80359537
Gnomad	rs80359537
Varsome	rs80359537
LitVar	rs80359537
Map	rs80359537
PheGenI	rs80359537
Biobank	rs80359537
1000 genomes	rs80359537
hgdp	rs80359537
ensembl	rs80359537
geneview	rs80359537
scholar	rs80359537
google	rs80359537
pharmgkb	rs80359537
gwascentral	rs80359537
openSNP	rs80359537
23andMe	rs80359537
SNPshot	rs80359537
SNPdbe	rs80359537
MSV3d	rs80359537
GWAS Ctlg	rs80359537

Max Magnitude

6

rs80359537, also known as 6024delTA, c.5796_5797delTA and p.His1932_Asn1933GlnProfs, is a variant in the BRCA2 gene considered pathogenic for breast cancer in ClinVar.

ClinVar
Risk	rs80359537(-;-) Rs80359537(AT;AT)
Alt	rs80359537(-;-) Rs80359537(AT;AT)
Reference	Rs80359537(TA;TA)
Significance	Pathogenic
Disease	Breast-ovarian cancer Hereditary cancer-predisposing syndrome Hereditary breast and ovarian cancer syndrome
Variation	info
Gene	BRCA2
CLNDBN	Breast-ovarian cancer, familial 2 Hereditary cancer-predisposing syndrome Hereditary breast and ovarian cancer syndrome
Reversed	0
HGVS	NC_000013.10:g.32914288_32914289delTA
CLNSRC	Breast Cancer Information Core (BRCA2)
CLNACC	RCV000113484.5, RCV000131106.3, RCV000257917.3,