rs80359726

plus

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

Make rs80359726(-;-)

Reference

GRCh38 38.1/141

Chromosome

13

Position

32376750

Gene

BRCA2

is a	snp
is	mentioned by
dbSNP	rs80359726
dbSNP (classic)	rs80359726
ClinGen	rs80359726
ebi	rs80359726
HLI	rs80359726
Exac	rs80359726
Gnomad	rs80359726
Varsome	rs80359726
LitVar	rs80359726
Map	rs80359726
PheGenI	rs80359726
Biobank	rs80359726
1000 genomes	rs80359726
hgdp	rs80359726
ensembl	rs80359726
geneview	rs80359726
scholar	rs80359726
google	rs80359726
pharmgkb	rs80359726
gwascentral	rs80359726
openSNP	rs80359726
23andMe	rs80359726
SNPshot	rs80359726
SNPdbe	rs80359726
MSV3d	rs80359726
GWAS Ctlg	rs80359726

Max Magnitude

6

rs80359726, also known as c.8713_8716delTATG, 8941del4, c.8713_8716delTATG and p.Tyr2905_Glu2906?fs, is a variant in the BRCA2 gene considered pathogenic for breast cancer in ClinVar.

ClinVar
Risk	rs80359726(-;-)
Alt	rs80359726(-;-)
Reference	Rs80359726(TATG;TATG)
Significance	Pathogenic
Disease	Familial cancer of breast Breast-ovarian cancer
Variation	info
Gene	BRCA2
CLNDBN	Familial cancer of breast Breast-ovarian cancer, familial 2
Reversed	0
HGVS	NC_000013.10:g.32950887_32950890delTATG
CLNSRC	Breast Cancer Information Core (BRCA2)
CLNACC	RCV000045606.2, RCV000113988.2,