rs398122789

Orientation

plus

Stabilized

plus

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

Make rs398122789(A;A)

Reference

GRCh38 38.1/141

Chromosome

13

Position

32339319

Gene

BRCA2

is a	snp
is	mentioned by
dbSNP	rs398122789
dbSNP (classic)	rs398122789
ClinGen	rs398122789
ebi	rs398122789
HLI	rs398122789
Exac	rs398122789
Gnomad	rs398122789
Varsome	rs398122789
LitVar	rs398122789
Map	rs398122789
PheGenI	rs398122789
Biobank	rs398122789
1000 genomes	rs398122789
hgdp	rs398122789
ensembl	rs398122789
geneview	rs398122789
scholar	rs398122789
google	rs398122789
pharmgkb	rs398122789
gwascentral	rs398122789
openSNP	rs398122789
23andMe	rs398122789
SNPshot	rs398122789
SNPdbe	rs398122789
MSV3d	rs398122789
GWAS Ctlg	rs398122789

Max Magnitude

6

ClinVar
Risk	rs398122789(A;A)
Alt	rs398122789(A;A)
Reference	Rs398122789(-;-)
Significance	Pathogenic
Disease	Breast-ovarian cancer Hereditary cancer-predisposing syndrome not provided
Variation	info
Gene	BRCA2
CLNDBN	Breast-ovarian cancer, familial 2 Hereditary cancer-predisposing syndrome not provided
Reversed	0
HGVS	NC_000013.10:g.32913456dupA
CLNSRC	ClinVar
CLNACC	RCV000077738.4, RCV000218684.1, RCV000480916.1,