rs397507601

Orientation

plus

Stabilized

plus

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

Make rs397507601(-;-)

Reference

GRCh38 38.1/141

Chromosome

13

Position

32333150

Gene

BRCA2

is a	snp
is	mentioned by
dbSNP	rs397507601
dbSNP (classic)	rs397507601
ClinGen	rs397507601
ebi	rs397507601
HLI	rs397507601
Exac	rs397507601
Gnomad	rs397507601
Varsome	rs397507601
LitVar	rs397507601
Map	rs397507601
PheGenI	rs397507601
Biobank	rs397507601
1000 genomes	rs397507601
hgdp	rs397507601
ensembl	rs397507601
geneview	rs397507601
scholar	rs397507601
google	rs397507601
pharmgkb	rs397507601
gwascentral	rs397507601
openSNP	rs397507601
23andMe	rs397507601
SNPshot	rs397507601
SNPdbe	rs397507601
MSV3d	rs397507601
GWAS Ctlg	rs397507601

Max Magnitude

6

ClinVar
Risk	rs397507601(-;-)
Alt	rs397507601(-;-)
Reference	Rs397507601(A;A)
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.32907287delA
CLNSRC	ClinVar
CLNACC	RCV000043859.2, RCV000241089.2,