rs398122790

Orientation

plus

Stabilized

plus

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

Make rs398122790(-;-)

Reference

GRCh38 38.1/141

Chromosome

13

Position

32339345

Gene

BRCA2

is a	snp
is	mentioned by
dbSNP	rs398122790
dbSNP (classic)	rs398122790
ClinGen	rs398122790
ebi	rs398122790
HLI	rs398122790
Exac	rs398122790
Gnomad	rs398122790
Varsome	rs398122790
LitVar	rs398122790
Map	rs398122790
PheGenI	rs398122790
Biobank	rs398122790
1000 genomes	rs398122790
hgdp	rs398122790
ensembl	rs398122790
geneview	rs398122790
scholar	rs398122790
google	rs398122790
pharmgkb	rs398122790
gwascentral	rs398122790
openSNP	rs398122790
23andMe	rs398122790
SNPshot	rs398122790
SNPdbe	rs398122790
MSV3d	rs398122790
GWAS Ctlg	rs398122790

Max Magnitude

6

ClinVar
Risk	rs398122790(-;-)
Alt	rs398122790(-;-)
Reference	Rs398122790(AT;AT)
Significance	Pathogenic
Disease	Breast-ovarian cancer
Variation	info
Gene	BRCA2
CLNDBN	Breast-ovarian cancer, familial 2
Reversed	0
HGVS	NC_000013.10:g.32913482_32913483delAT
CLNSRC	ClinVar
CLNACC	RCV000077739.3,