rs398122777

Orientation

plus

Stabilized

plus

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

Make rs398122777(-;-)

Reference

GRCh38 38.1/141

Chromosome

13

Position

32338566

Gene

BRCA2

is a	snp
is	mentioned by
dbSNP	rs398122777
dbSNP (classic)	rs398122777
ClinGen	rs398122777
ebi	rs398122777
HLI	rs398122777
Exac	rs398122777
Gnomad	rs398122777
Varsome	rs398122777
LitVar	rs398122777
Map	rs398122777
PheGenI	rs398122777
Biobank	rs398122777
1000 genomes	rs398122777
hgdp	rs398122777
ensembl	rs398122777
geneview	rs398122777
scholar	rs398122777
google	rs398122777
pharmgkb	rs398122777
gwascentral	rs398122777
openSNP	rs398122777
23andMe	rs398122777
SNPshot	rs398122777
SNPdbe	rs398122777
MSV3d	rs398122777
GWAS Ctlg	rs398122777

Max Magnitude

6

ClinVar
Risk	rs398122777(-;-)
Alt	rs398122777(-;-)
Reference	Rs398122777(C;C)
Significance	Pathogenic
Disease	Breast-ovarian cancer Hereditary breast and ovarian cancer syndrome not provided
Variation	info
Gene	BRCA2
CLNDBN	Breast-ovarian cancer, familial 2 Hereditary breast and ovarian cancer syndrome not provided
Reversed	0
HGVS	NC_000013.10:g.32912703delC
CLNSRC	ClinVar
CLNACC	RCV000077723.4, RCV000462802.1, RCV000478663.1,