rs398122744

Orientation

plus

Stabilized

plus

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

Make rs398122744(-;-)

Reference

GRCh38 38.1/141

Chromosome

13

Position

32336608

Gene

BRCA2

is a	snp
is	mentioned by
dbSNP	rs398122744
dbSNP (classic)	rs398122744
ClinGen	rs398122744
ebi	rs398122744
HLI	rs398122744
Exac	rs398122744
Gnomad	rs398122744
Varsome	rs398122744
LitVar	rs398122744
Map	rs398122744
PheGenI	rs398122744
Biobank	rs398122744
1000 genomes	rs398122744
hgdp	rs398122744
ensembl	rs398122744
geneview	rs398122744
scholar	rs398122744
google	rs398122744
pharmgkb	rs398122744
gwascentral	rs398122744
openSNP	rs398122744
23andMe	rs398122744
SNPshot	rs398122744
SNPdbe	rs398122744
MSV3d	rs398122744
GWAS Ctlg	rs398122744

Max Magnitude

6

ClinVar
Risk	rs398122744(-;-)
Alt	rs398122744(-;-)
Reference	Rs398122744(TG;TG)
Significance	Pathogenic
Disease	Breast-ovarian cancer not provided
Variation	info
Gene	BRCA2
CLNDBN	Breast-ovarian cancer, familial 2 not provided
Reversed	0
HGVS	NC_000013.10:g.32910745_32910746delTG
CLNSRC	ClinVar
CLNACC	RCV000077681.3, RCV000481582.1,