rs397507774

Orientation

plus

Stabilized

plus

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

Make rs397507774(-;-)

Reference

GRCh38 38.1/141

Chromosome

13

Position

32339563

Gene

BRCA2

is a	snp
is	mentioned by
dbSNP	rs397507774
dbSNP (classic)	rs397507774
ClinGen	rs397507774
ebi	rs397507774
HLI	rs397507774
Exac	rs397507774
Gnomad	rs397507774
Varsome	rs397507774
LitVar	rs397507774
Map	rs397507774
PheGenI	rs397507774
Biobank	rs397507774
1000 genomes	rs397507774
hgdp	rs397507774
ensembl	rs397507774
geneview	rs397507774
scholar	rs397507774
google	rs397507774
pharmgkb	rs397507774
gwascentral	rs397507774
openSNP	rs397507774
23andMe	rs397507774
SNPshot	rs397507774
SNPdbe	rs397507774
MSV3d	rs397507774
GWAS Ctlg	rs397507774

Max Magnitude

6

ClinVar
Risk	rs397507774(-;-)
Alt	rs397507774(-;-)
Reference	Rs397507774(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.32913700delA
CLNSRC	ClinVar
CLNACC	RCV000044607.2, RCV000256578.2,