rs397507652

Orientation

plus

Stabilized

plus

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

Make rs397507652(T;T)

Reference

GRCh38 38.1/141

Chromosome

13

Position

32337398

Gene

BRCA2

is a	snp
is	mentioned by
dbSNP	rs397507652
dbSNP (classic)	rs397507652
ClinGen	rs397507652
ebi	rs397507652
HLI	rs397507652
Exac	rs397507652
Gnomad	rs397507652
Varsome	rs397507652
LitVar	rs397507652
Map	rs397507652
PheGenI	rs397507652
Biobank	rs397507652
1000 genomes	rs397507652
hgdp	rs397507652
ensembl	rs397507652
geneview	rs397507652
scholar	rs397507652
google	rs397507652
pharmgkb	rs397507652
gwascentral	rs397507652
openSNP	rs397507652
23andMe	rs397507652
SNPshot	rs397507652
SNPdbe	rs397507652
MSV3d	rs397507652
GWAS Ctlg	rs397507652

Max Magnitude

6

ClinVar
Risk	rs397507652(T;T)
Alt	rs397507652(T;T)
Reference	Rs397507652(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.32911535A>T
CLNSRC	ClinVar
CLNACC	RCV000044106.2, RCV000256630.2,