rs397507749

Orientation

plus

Stabilized

plus

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

Make rs397507749(-;-)

Reference

GRCh38 38.1/141

Chromosome

13

Position

32339272

Gene

BRCA2

is a	snp
is	mentioned by
dbSNP	rs397507749
dbSNP (classic)	rs397507749
ClinGen	rs397507749
ebi	rs397507749
HLI	rs397507749
Exac	rs397507749
Gnomad	rs397507749
Varsome	rs397507749
LitVar	rs397507749
Map	rs397507749
PheGenI	rs397507749
Biobank	rs397507749
1000 genomes	rs397507749
hgdp	rs397507749
ensembl	rs397507749
geneview	rs397507749
scholar	rs397507749
google	rs397507749
pharmgkb	rs397507749
gwascentral	rs397507749
openSNP	rs397507749
23andMe	rs397507749
SNPshot	rs397507749
SNPdbe	rs397507749
MSV3d	rs397507749
GWAS Ctlg	rs397507749

Max Magnitude

6

aka c.4917delA

ClinVar
Risk	rs397507749(-;-)
Alt	rs397507749(-;-)
Reference	Rs397507749(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.32913409delA
CLNSRC	ClinVar
CLNACC	RCV000044520.2,