rs398122610

Orientation

plus

Stabilized

plus

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

Make rs398122610(T;T)

Reference

GRCh38 38.1/141

Chromosome

13

Position

32380016

Gene

BRCA2

is a	snp
is	mentioned by
dbSNP	rs398122610
dbSNP (classic)	rs398122610
ClinGen	rs398122610
ebi	rs398122610
HLI	rs398122610
Exac	rs398122610
Gnomad	rs398122610
Varsome	rs398122610
LitVar	rs398122610
Map	rs398122610
PheGenI	rs398122610
Biobank	rs398122610
1000 genomes	rs398122610
hgdp	rs398122610
ensembl	rs398122610
geneview	rs398122610
scholar	rs398122610
google	rs398122610
pharmgkb	rs398122610
gwascentral	rs398122610
openSNP	rs398122610
23andMe	rs398122610
SNPshot	rs398122610
SNPdbe	rs398122610
MSV3d	rs398122610
GWAS Ctlg	rs398122610

Max Magnitude

6

ClinVar
Risk	rs398122610(T;T)
Alt	rs398122610(T;T)
Reference	Rs398122610(G;G)
Significance	Pathogenic
Disease	Breast-ovarian cancer Hereditary cancer-predisposing syndrome
Variation	info
Gene	BRCA2
CLNDBN	Breast-ovarian cancer, familial 2 Hereditary cancer-predisposing syndrome
Reversed	0
HGVS	NC_000013.10:g.32954153G>T
CLNSRC	Ambry Genetics ClinVar
CLNACC	RCV000077034.4, RCV000130444.3,