rs397507699

Orientation

plus

Stabilized

plus

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

Make rs397507699(-;-)

Reference

GRCh38 38.1/141

Chromosome

13

Position

32338284

Gene

BRCA2

is a	snp
is	mentioned by
dbSNP	rs397507699
dbSNP (classic)	rs397507699
ClinGen	rs397507699
ebi	rs397507699
HLI	rs397507699
Exac	rs397507699
Gnomad	rs397507699
Varsome	rs397507699
LitVar	rs397507699
Map	rs397507699
PheGenI	rs397507699
Biobank	rs397507699
1000 genomes	rs397507699
hgdp	rs397507699
ensembl	rs397507699
geneview	rs397507699
scholar	rs397507699
google	rs397507699
pharmgkb	rs397507699
gwascentral	rs397507699
openSNP	rs397507699
23andMe	rs397507699
SNPshot	rs397507699
SNPdbe	rs397507699
MSV3d	rs397507699
GWAS Ctlg	rs397507699

Max Magnitude

6

aka c.3929delC (p.Thr1310fs)

ClinVar
Risk	rs397507699(-;-)
Alt	rs397507699(-;-)
Reference	Rs397507699(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.32912421delC
CLNSRC	ClinVar
CLNACC	RCV000044313.2,