rs398122622

Orientation

plus

Stabilized

plus

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

Make rs398122622(-;-)

Reference

GRCh38 38.1/141

Chromosome

13

Position

32398321

Gene

BRCA2

is a	snp
is	mentioned by
dbSNP	rs398122622
dbSNP (classic)	rs398122622
ClinGen	rs398122622
ebi	rs398122622
HLI	rs398122622
Exac	rs398122622
Gnomad	rs398122622
Varsome	rs398122622
LitVar	rs398122622
Map	rs398122622
PheGenI	rs398122622
Biobank	rs398122622
1000 genomes	rs398122622
hgdp	rs398122622
ensembl	rs398122622
geneview	rs398122622
scholar	rs398122622
google	rs398122622
pharmgkb	rs398122622
gwascentral	rs398122622
openSNP	rs398122622
23andMe	rs398122622
SNPshot	rs398122622
SNPdbe	rs398122622
MSV3d	rs398122622
GWAS Ctlg	rs398122622

Max Magnitude

6

ClinVar
Risk	rs398122622(-;-)
Alt	rs398122622(-;-)
Reference	Rs398122622(G;G)
Significance	Pathogenic
Disease	Breast-ovarian cancer Hereditary breast and ovarian cancer syndrome Hereditary cancer-predisposing syndrome
Variation	info
Gene	BRCA2
CLNDBN	Breast-ovarian cancer, familial 2 Hereditary breast and ovarian cancer syndrome Hereditary cancer-predisposing syndrome
Reversed	0
HGVS	NC_000013.10:g.32972458delG
CLNSRC	ClinVar
CLNACC	RCV000077051.4, RCV000197732.1, RCV000217558.1,