rs398122618

Orientation

plus

Stabilized

plus

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

Make rs398122618(-;-)

Reference

GRCh38 38.1/141

Chromosome

13

Position

32398195

Gene

BRCA2

is a	snp
is	mentioned by
dbSNP	rs398122618
dbSNP (classic)	rs398122618
ClinGen	rs398122618
ebi	rs398122618
HLI	rs398122618
Exac	rs398122618
Gnomad	rs398122618
Varsome	rs398122618
LitVar	rs398122618
Map	rs398122618
PheGenI	rs398122618
Biobank	rs398122618
1000 genomes	rs398122618
hgdp	rs398122618
ensembl	rs398122618
geneview	rs398122618
scholar	rs398122618
google	rs398122618
pharmgkb	rs398122618
gwascentral	rs398122618
openSNP	rs398122618
23andMe	rs398122618
SNPshot	rs398122618
SNPdbe	rs398122618
MSV3d	rs398122618
GWAS Ctlg	rs398122618

Max Magnitude

6

ClinVar
Risk	rs398122618(-;-)
Alt	rs398122618(-;-)
Reference	Rs398122618(A;A)
Significance	Pathogenic
Disease	Breast-ovarian cancer
Variation	info
Gene	BRCA2
CLNDBN	Breast-ovarian cancer, familial 2
Reversed	0
HGVS	NC_000013.10:g.32972332delA
CLNSRC	ClinVar
CLNACC	RCV000077047.4,