rs397507621

Orientation

plus

Stabilized

plus

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

Make rs397507621(-;-)

Reference

GRCh38 38.1/141

Chromosome

13

Position

32336614

Gene

BRCA2

is a	snp
is	mentioned by
dbSNP	rs397507621
ClinGen	rs397507621
ebi	rs397507621
HLI	rs397507621
Exac	rs397507621
Varsome	rs397507621
Map	rs397507621
PheGenI	rs397507621
hapmap	rs397507621
1000 genomes	rs397507621
hgdp	rs397507621
ensembl	rs397507621
gopubmed	rs397507621
geneview	rs397507621
scholar	rs397507621
google	rs397507621
pharmgkb	rs397507621
gwascentral	rs397507621
openSNP	rs397507621
23andMe	rs397507621
23andMe all	rs397507621
SNP Nexus
SNPshot	rs397507621
SNPdbe	rs397507621
MSV3d	rs397507621
GWAS Ctlg	rs397507621

Max Magnitude

6

ClinVar
Risk	rs397507621(-;-)
Alt	rs397507621(-;-)
Reference	Rs397507621(T;T)
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.32910751delT
CLNSRC	ClinVar
CLNACC	RCV000043963.2, RCV000257171.2,