rs398122561

Orientation

plus

Stabilized

plus

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

Make rs398122561(T;T)

Reference

GRCh38 38.1/141

Chromosome

13

Position

32340941

Gene

BRCA2

is a	snp
is	mentioned by
dbSNP	rs398122561
dbSNP (classic)	rs398122561
ClinGen	rs398122561
ebi	rs398122561
HLI	rs398122561
Exac	rs398122561
Gnomad	rs398122561
Varsome	rs398122561
LitVar	rs398122561
Map	rs398122561
PheGenI	rs398122561
Biobank	rs398122561
1000 genomes	rs398122561
hgdp	rs398122561
ensembl	rs398122561
geneview	rs398122561
scholar	rs398122561
google	rs398122561
pharmgkb	rs398122561
gwascentral	rs398122561
openSNP	rs398122561
23andMe	rs398122561
SNPshot	rs398122561
SNPdbe	rs398122561
MSV3d	rs398122561
GWAS Ctlg	rs398122561

Max Magnitude

6

ClinVar
Risk	rs398122561(T;T)
Alt	rs398122561(T;T)
Reference	Rs398122561(A;A)
Significance	Pathogenic
Disease	Breast-ovarian cancer
Variation	info
Gene	BRCA2
CLNDBN	Breast-ovarian cancer, familial 2
Reversed	0
HGVS	NC_000013.10:g.32915078A>T
CLNSRC	ClinVar
CLNACC	RCV000076970.3,