rs398122742

Orientation

plus

Stabilized

plus

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

Make rs398122742(A;A)

Reference

GRCh38 38.1/141

Chromosome

13

Position

32336569

Gene

BRCA2

is a	snp
is	mentioned by
dbSNP	rs398122742
dbSNP (classic)	rs398122742
ClinGen	rs398122742
ebi	rs398122742
HLI	rs398122742
Exac	rs398122742
Gnomad	rs398122742
Varsome	rs398122742
LitVar	rs398122742
Map	rs398122742
PheGenI	rs398122742
Biobank	rs398122742
1000 genomes	rs398122742
hgdp	rs398122742
ensembl	rs398122742
geneview	rs398122742
scholar	rs398122742
google	rs398122742
pharmgkb	rs398122742
gwascentral	rs398122742
openSNP	rs398122742
23andMe	rs398122742
SNPshot	rs398122742
SNPdbe	rs398122742
MSV3d	rs398122742
GWAS Ctlg	rs398122742

Max Magnitude

6

ClinVar
Risk	rs398122742(A;A)
Alt	rs398122742(A;A)
Reference	Rs398122742(T;T)
Significance	Pathogenic
Disease	Breast-ovarian cancer
Variation	info
Gene	BRCA2
CLNDBN	Breast-ovarian cancer, familial 2
Reversed	0
HGVS	NC_000013.10:g.32910706T>A
CLNSRC	ClinVar
CLNACC	RCV000077679.5,