rs397508032

Orientation

plus

Stabilized

plus

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

Make rs397508032(-;-)

Reference

GRCh38 38.1/141

Chromosome

13

Position

32379859

Gene

BRCA2

is a	snp
is	mentioned by
dbSNP	rs397508032
dbSNP (classic)	rs397508032
ClinGen	rs397508032
ebi	rs397508032
HLI	rs397508032
Exac	rs397508032
Gnomad	rs397508032
Varsome	rs397508032
LitVar	rs397508032
Map	rs397508032
PheGenI	rs397508032
Biobank	rs397508032
1000 genomes	rs397508032
hgdp	rs397508032
ensembl	rs397508032
geneview	rs397508032
scholar	rs397508032
google	rs397508032
pharmgkb	rs397508032
gwascentral	rs397508032
openSNP	rs397508032
23andMe	rs397508032
SNPshot	rs397508032
SNPdbe	rs397508032
MSV3d	rs397508032
GWAS Ctlg	rs397508032

Max Magnitude

6

ClinVar
Risk	rs397508032(-;-)
Alt	rs397508032(-;-)
Reference	Rs397508032(AAGAGCTAACATACAG;AAGAGCTAACATACAG)
Significance	Pathogenic
Disease	Familial cancer of breast Breast-ovarian cancer
Variation	info
Gene	BRCA2
CLNDBN	Familial cancer of breast Breast-ovarian cancer, familial 2
Reversed	0
HGVS	NC_000013.10:g.32953996_32954011del16
CLNSRC	ClinVar
CLNACC	RCV000045701.2, RCV000241311.2,