rs397507619

Orientation

plus

Stabilized

plus

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

Make rs397507619(TT;TT)

Reference

GRCh38 38.1/141

Chromosome

13

Position

32319224

Gene

BRCA2

is a	snp
is	mentioned by
dbSNP	rs397507619
dbSNP (classic)	rs397507619
ClinGen	rs397507619
ebi	rs397507619
HLI	rs397507619
Exac	rs397507619
Gnomad	rs397507619
Varsome	rs397507619
LitVar	rs397507619
Map	rs397507619
PheGenI	rs397507619
Biobank	rs397507619
1000 genomes	rs397507619
hgdp	rs397507619
ensembl	rs397507619
geneview	rs397507619
scholar	rs397507619
google	rs397507619
pharmgkb	rs397507619
gwascentral	rs397507619
openSNP	rs397507619
23andMe	rs397507619
SNPshot	rs397507619
SNPdbe	rs397507619
MSV3d	rs397507619
GWAS Ctlg	rs397507619

Max Magnitude

6

ClinVar
Risk	rs397507619(TT;TT)
Alt	rs397507619(TT;TT)
Reference	Rs397507619(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.32893361delAinsTT
CLNSRC	ClinVar
CLNACC	RCV000043953.2, RCV000225535.2,