rs397507665

Orientation

plus

Stabilized

plus

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

Make rs397507665(-;-)

Reference

GRCh38 38.1/141

Chromosome

13

Position

32337721

Gene

BRCA2

is a	snp
is	mentioned by
dbSNP	rs397507665
dbSNP (classic)	rs397507665
ClinGen	rs397507665
ebi	rs397507665
HLI	rs397507665
Exac	rs397507665
Gnomad	rs397507665
Varsome	rs397507665
LitVar	rs397507665
Map	rs397507665
PheGenI	rs397507665
Biobank	rs397507665
1000 genomes	rs397507665
hgdp	rs397507665
ensembl	rs397507665
geneview	rs397507665
scholar	rs397507665
google	rs397507665
pharmgkb	rs397507665
gwascentral	rs397507665
openSNP	rs397507665
23andMe	rs397507665
SNPshot	rs397507665
SNPdbe	rs397507665
MSV3d	rs397507665
GWAS Ctlg	rs397507665

Max Magnitude

6

aka c.3366_3367delAA (p.Gln1124fs)

ClinVar
Risk	rs397507665(-;-)
Alt	rs397507665(-;-)
Reference	Rs397507665(AA;AA)
Significance	Untested
Disease	Familial cancer of breast
Variation	info
Gene	BRCA2
CLNDBN	Familial cancer of breast
Reversed	0
HGVS	NC_000013.10:g.32911858_32911859delAA
CLNSRC	ClinVar
CLNACC	RCV000044182.2,