rs397507569

Orientation

plus

Stabilized

plus

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

Make rs397507569(-;-)

Reference

GRCh38 38.1/141

Chromosome

13

Position

32332560

Gene

BRCA2

is a	snp
is	mentioned by
dbSNP	rs397507569
dbSNP (classic)	rs397507569
ClinGen	rs397507569
ebi	rs397507569
HLI	rs397507569
Exac	rs397507569
Gnomad	rs397507569
Varsome	rs397507569
LitVar	rs397507569
Map	rs397507569
PheGenI	rs397507569
Biobank	rs397507569
1000 genomes	rs397507569
hgdp	rs397507569
ensembl	rs397507569
geneview	rs397507569
scholar	rs397507569
google	rs397507569
pharmgkb	rs397507569
gwascentral	rs397507569
openSNP	rs397507569
23andMe	rs397507569
SNPshot	rs397507569
SNPdbe	rs397507569
MSV3d	rs397507569
GWAS Ctlg	rs397507569

Max Magnitude

6

aka c.1082delA (p.Asn361fs)

ClinVar
Risk	rs397507569(-;-)
Alt	rs397507569(-;-)
Reference	Rs397507569(A;A)
Significance	Untested
Disease	Familial cancer of breast
Variation	info
Gene	BRCA2
CLNDBN	Familial cancer of breast
Reversed	0
HGVS	NC_000013.10:g.32906697delA
CLNSRC	ClinVar
CLNACC	RCV000043735.2,