rs397507396

Orientation

plus

Stabilized

plus

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

Make rs397507396(-;-)

Reference

GRCh38 38.1/141

Chromosome

13

Position

32363407

Gene

BRCA2

is a	snp
is	mentioned by
dbSNP	rs397507396
dbSNP (classic)	rs397507396
ClinGen	rs397507396
ebi	rs397507396
HLI	rs397507396
Exac	rs397507396
Gnomad	rs397507396
Varsome	rs397507396
LitVar	rs397507396
Map	rs397507396
PheGenI	rs397507396
Biobank	rs397507396
1000 genomes	rs397507396
hgdp	rs397507396
ensembl	rs397507396
geneview	rs397507396
scholar	rs397507396
google	rs397507396
pharmgkb	rs397507396
gwascentral	rs397507396
openSNP	rs397507396
23andMe	rs397507396
SNPshot	rs397507396
SNPdbe	rs397507396
MSV3d	rs397507396
GWAS Ctlg	rs397507396

Max Magnitude

6

ClinVar
Risk	rs397507396(-;-)
Alt	rs397507396(-;-)
Reference	Rs397507396(CC;CC)
Significance	Pathogenic
Disease	Breast-ovarian cancer not provided
Variation	info
Gene	BRCA2
CLNDBN	Breast-ovarian cancer, familial 2 not provided
Reversed	0
HGVS	NC_000013.10:g.32937544_32937545delCC
CLNSRC	ClinVar
CLNACC	RCV000031726.5, RCV000479269.1,