rs397507776

Orientation

plus

Stabilized

plus

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

Make rs397507776(-;-)

Reference

GRCh38 38.1/141

Chromosome

13

Position

32339605

Gene

BRCA2

is a	snp
is	mentioned by
dbSNP	rs397507776
dbSNP (classic)	rs397507776
ClinGen	rs397507776
ebi	rs397507776
HLI	rs397507776
Exac	rs397507776
Gnomad	rs397507776
Varsome	rs397507776
LitVar	rs397507776
Map	rs397507776
PheGenI	rs397507776
Biobank	rs397507776
1000 genomes	rs397507776
hgdp	rs397507776
ensembl	rs397507776
geneview	rs397507776
scholar	rs397507776
google	rs397507776
pharmgkb	rs397507776
gwascentral	rs397507776
openSNP	rs397507776
23andMe	rs397507776
SNPshot	rs397507776
SNPdbe	rs397507776
MSV3d	rs397507776
GWAS Ctlg	rs397507776

Max Magnitude

6

aka c.5250delC

ClinVar
Risk	rs397507776(-;-)
Alt	rs397507776(-;-)
Reference	Rs397507776(C;C)
Significance	Untested
Disease	Familial cancer of breast
Variation	info
Gene	BRCA2
CLNDBN	Familial cancer of breast
Reversed	0
HGVS	NC_000013.10:g.32913742delC
CLNSRC	ClinVar
CLNACC	RCV000044620.2,