rs398122735

Orientation

plus

Stabilized

plus

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

Make rs398122735(T;T)

Reference

GRCh38 38.1/141

Chromosome

13

Position

32336300

Gene

BRCA2

is a	snp
is	mentioned by
dbSNP	rs398122735
dbSNP (classic)	rs398122735
ClinGen	rs398122735
ebi	rs398122735
HLI	rs398122735
Exac	rs398122735
Gnomad	rs398122735
Varsome	rs398122735
LitVar	rs398122735
Map	rs398122735
PheGenI	rs398122735
Biobank	rs398122735
1000 genomes	rs398122735
hgdp	rs398122735
ensembl	rs398122735
geneview	rs398122735
scholar	rs398122735
google	rs398122735
pharmgkb	rs398122735
gwascentral	rs398122735
openSNP	rs398122735
23andMe	rs398122735
SNPshot	rs398122735
SNPdbe	rs398122735
MSV3d	rs398122735
GWAS Ctlg	rs398122735

Max Magnitude

6

ClinVar
Risk	rs398122735(T;T)
Alt	rs398122735(T;T)
Reference	Rs398122735(C;C)
Significance	Pathogenic
Disease	Breast-ovarian cancer
Variation	info
Gene	BRCA2
CLNDBN	Breast-ovarian cancer, familial 2
Reversed	0
HGVS	NC_000013.10:g.32910437C>T
CLNSRC	ClinVar
CLNACC	RCV000077672.4,