rs75096777

Orientation

plus

Stabilized

plus

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

Make rs75096777(-;-)

Reference

GRCh38 38.1/141

Chromosome

13

Position

32331012

Gene

BRCA2

is a	snp
is	mentioned by
dbSNP	rs75096777
dbSNP (classic)	rs75096777
ClinGen	rs75096777
ebi	rs75096777
HLI	rs75096777
Exac	rs75096777
Gnomad	rs75096777
Varsome	rs75096777
LitVar	rs75096777
Map	rs75096777
PheGenI	rs75096777
Biobank	rs75096777
1000 genomes	rs75096777
hgdp	rs75096777
ensembl	rs75096777
geneview	rs75096777
scholar	rs75096777
google	rs75096777
pharmgkb	rs75096777
gwascentral	rs75096777
openSNP	rs75096777
23andMe	rs75096777
SNPshot	rs75096777
SNPdbe	rs75096777
MSV3d	rs75096777
GWAS Ctlg	rs75096777

Max Magnitude

6

ClinVar
Risk	rs75096777(-;-)
Alt	rs75096777(-;-)
Reference	Rs75096777(A;A)
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.32905149delA
CLNSRC	ClinVar
CLNACC	RCV000045305.2, RCV000257570.1,