rs397507769

Orientation

plus

Stabilized

plus

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

Make rs397507769(A;A)

Reference

GRCh38 38.1/141

Chromosome

13

Position

32339535

Gene

BRCA2

is a	snp
is	mentioned by
dbSNP	rs397507769
dbSNP (classic)	rs397507769
ClinGen	rs397507769
ebi	rs397507769
HLI	rs397507769
Exac	rs397507769
Gnomad	rs397507769
Varsome	rs397507769
LitVar	rs397507769
Map	rs397507769
PheGenI	rs397507769
Biobank	rs397507769
1000 genomes	rs397507769
hgdp	rs397507769
ensembl	rs397507769
geneview	rs397507769
scholar	rs397507769
google	rs397507769
pharmgkb	rs397507769
gwascentral	rs397507769
openSNP	rs397507769
23andMe	rs397507769
SNPshot	rs397507769
SNPdbe	rs397507769
MSV3d	rs397507769
GWAS Ctlg	rs397507769

Max Magnitude

6

ClinVar
Risk	rs397507769(A;A)
Alt	rs397507769(A;A)
Reference	Rs397507769(-;-)
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.32913672dupA
CLNSRC	ClinVar
CLNACC	RCV000044595.2, RCV000256850.2,