rs80359388

plus

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

Make rs80359388(-;-)

Reference

GRCh38 38.1/141

Chromosome

13

Position

32337900

Gene

BRCA2

is a	snp
is	mentioned by
dbSNP	rs80359388
dbSNP (classic)	rs80359388
ClinGen	rs80359388
ebi	rs80359388
HLI	rs80359388
Exac	rs80359388
Gnomad	rs80359388
Varsome	rs80359388
LitVar	rs80359388
Map	rs80359388
PheGenI	rs80359388
Biobank	rs80359388
1000 genomes	rs80359388
hgdp	rs80359388
ensembl	rs80359388
geneview	rs80359388
scholar	rs80359388
google	rs80359388
pharmgkb	rs80359388
gwascentral	rs80359388
openSNP	rs80359388
23andMe	rs80359388
SNPshot	rs80359388
SNPdbe	rs80359388
MSV3d	rs80359388
GWAS Ctlg	rs80359388

Max Magnitude

6

rs80359388, also known as 3773delTT, c.3545_3546delTT and p.Phe1182Terfs, is a variant in the BRCA2 gene considered pathogenic for breast cancer in ClinVar.

23andMe name: i5009173

ClinVar
Risk	rs80359388(-;-)
Alt	rs80359388(-;-)
Reference	Rs80359388(TT;TT)
Significance	Pathogenic
Disease	Breast-ovarian cancer Hereditary breast and ovarian cancer syndrome not provided Hereditary cancer-predisposing syndrome Inborn genetic diseases
Variation	info
Gene	BRCA2
CLNDBN	Breast-ovarian cancer, familial 2 Hereditary breast and ovarian cancer syndrome not provided Hereditary cancer-predisposing syndrome Inborn genetic diseases
Reversed	0
HGVS	NC_000013.10:g.32912037_32912038delTT
CLNSRC	Breast Cancer Information Core (BRCA2)
CLNACC	RCV000031427.12, RCV000044219.4, RCV000074527.7, RCV000131093.3, RCV000210566.1,