rs398122775

Orientation

plus

Stabilized

plus

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

Make rs398122775(-;-)

Reference

GRCh38 38.1/141

Chromosome

13

Position

32338355

Gene

BRCA2

is a	snp
is	mentioned by
dbSNP	rs398122775
dbSNP (classic)	rs398122775
ClinGen	rs398122775
ebi	rs398122775
HLI	rs398122775
Exac	rs398122775
Gnomad	rs398122775
Varsome	rs398122775
LitVar	rs398122775
Map	rs398122775
PheGenI	rs398122775
Biobank	rs398122775
1000 genomes	rs398122775
hgdp	rs398122775
ensembl	rs398122775
geneview	rs398122775
scholar	rs398122775
google	rs398122775
pharmgkb	rs398122775
gwascentral	rs398122775
openSNP	rs398122775
23andMe	rs398122775
SNPshot	rs398122775
SNPdbe	rs398122775
MSV3d	rs398122775
GWAS Ctlg	rs398122775

Max Magnitude

6

ClinVar
Risk	rs398122775(-;-)
Alt	rs398122775(-;-)
Reference	Rs398122775(TT;TT)
Significance	Pathogenic
Disease	Breast-ovarian cancer Familial cancer of breast
Variation	info
Gene	BRCA2
CLNDBN	Breast-ovarian cancer, familial 2 Familial cancer of breast
Reversed	0
HGVS	NC_000013.10:g.32912492_32912493delTT
CLNSRC	ClinVar
CLNACC	RCV000077720.3, RCV000160282.1,