rs80359544

plus

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

Make rs80359544(-;-)

Reference

GRCh38 38.1/141

Chromosome

13

Position

32340206

Gene

BRCA2

is a	snp
is	mentioned by
dbSNP	rs80359544
dbSNP (classic)	rs80359544
ClinGen	rs80359544
ebi	rs80359544
HLI	rs80359544
Exac	rs80359544
Gnomad	rs80359544
Varsome	rs80359544
LitVar	rs80359544
Map	rs80359544
PheGenI	rs80359544
Biobank	rs80359544
1000 genomes	rs80359544
hgdp	rs80359544
ensembl	rs80359544
geneview	rs80359544
scholar	rs80359544
google	rs80359544
pharmgkb	rs80359544
gwascentral	rs80359544
openSNP	rs80359544
23andMe	rs80359544
SNPshot	rs80359544
SNPdbe	rs80359544
MSV3d	rs80359544
GWAS Ctlg	rs80359544

Status

Merged into rs80359543

Max Magnitude

6

rs80359544, also known as 6079del4, c.5851_5854delAGTT and p.Ser1951_Leu1952?fs, is a variant in the BRCA2 gene considered pathogenic for breast cancer in ClinVar.

ClinVar
Risk
Alt
Reference	Rs80359544(GTTA;GTTA)
Significance	Pathogenic
Disease	Breast-ovarian cancer Familial cancer of breast Hereditary cancer-predisposing syndrome not provided
Variation	info
Gene	BRCA2
CLNDBN	Breast-ovarian cancer, familial 2 Familial cancer of breast Hereditary cancer-predisposing syndrome not provided
Reversed	0
HGVS	NC_000013.10:g.32914343_32914346delAGTT
CLNSRC	Breast Cancer Information Core (BRCA2)
CLNACC	RCV000031582.10, RCV000044773.3, RCV000131116.3, RCV000254645.1,