rs397508041

Orientation

plus

Stabilized

plus

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

Make rs397508041(-;-)

Reference

GRCh38 38.1/141

Chromosome

13

Position

32380142

Gene

BRCA2

is a	snp
is	mentioned by
dbSNP	rs397508041
dbSNP (classic)	rs397508041
ClinGen	rs397508041
ebi	rs397508041
HLI	rs397508041
Exac	rs397508041
Gnomad	rs397508041
Varsome	rs397508041
LitVar	rs397508041
Map	rs397508041
PheGenI	rs397508041
Biobank	rs397508041
1000 genomes	rs397508041
hgdp	rs397508041
ensembl	rs397508041
geneview	rs397508041
scholar	rs397508041
google	rs397508041
pharmgkb	rs397508041
gwascentral	rs397508041
openSNP	rs397508041
23andMe	rs397508041
SNPshot	rs397508041
SNPdbe	rs397508041
MSV3d	rs397508041
GWAS Ctlg	rs397508041

Max Magnitude

6

ClinVar
Risk	rs397508041(-;-)
Alt	rs397508041(-;-)
Reference	Rs397508041(A;A)
Significance	Pathogenic
Disease	Hereditary breast and ovarian cancer syndrome not provided Breast-ovarian cancer
Variation	info
Gene	BRCA2
CLNDBN	Hereditary breast and ovarian cancer syndrome not provided Breast-ovarian cancer, familial 2
Reversed	0
HGVS	NC_000013.10:g.32954279delA
CLNSRC	ClinVar
CLNACC	RCV000045759.3, RCV000236478.2, RCV000257577.2,