rs730881610

Orientation

plus

Stabilized

plus

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

Make rs730881610(-;-)

Reference

GRCh38.p2 38.2/144

Chromosome

13

Position

32339179

Gene

BRCA2

is a	snp
is	mentioned by
dbSNP	rs730881610
dbSNP (classic)	rs730881610
ClinGen	rs730881610
ebi	rs730881610
HLI	rs730881610
Exac	rs730881610
Gnomad	rs730881610
Varsome	rs730881610
LitVar	rs730881610
Map	rs730881610
PheGenI	rs730881610
Biobank	rs730881610
1000 genomes	rs730881610
hgdp	rs730881610
ensembl	rs730881610
geneview	rs730881610
scholar	rs730881610
google	rs730881610
pharmgkb	rs730881610
gwascentral	rs730881610
openSNP	rs730881610
23andMe	rs730881610
SNPshot	rs730881610
SNPdbe	rs730881610
MSV3d	rs730881610
GWAS Ctlg	rs730881610

Max Magnitude

6

ClinVar
Risk	rs730881610(-;-)
Alt	rs730881610(-;-)
Reference	Rs730881610(GA;GA)
Significance	Pathogenic
Disease	not provided Breast-ovarian cancer
Variation	info
Gene	BRCA2
CLNDBN	not provided Breast-ovarian cancer, familial 2
Reversed	0
HGVS	NC_000013.10:g.32913316_32913317delGA
CLNSRC
CLNACC	RCV000160292.2, RCV000241101.1,