rs730881613

Orientation

plus

Stabilized

plus

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

Make rs730881613(-;-)

Reference

GRCh38.p2 38.2/144

Chromosome

13

Position

32356580

Gene

BRCA2

is a	snp
is	mentioned by
dbSNP	rs730881613
dbSNP (classic)	rs730881613
ClinGen	rs730881613
ebi	rs730881613
HLI	rs730881613
Exac	rs730881613
Gnomad	rs730881613
Varsome	rs730881613
LitVar	rs730881613
Map	rs730881613
PheGenI	rs730881613
Biobank	rs730881613
1000 genomes	rs730881613
hgdp	rs730881613
ensembl	rs730881613
geneview	rs730881613
scholar	rs730881613
google	rs730881613
pharmgkb	rs730881613
gwascentral	rs730881613
openSNP	rs730881613
23andMe	rs730881613
SNPshot	rs730881613
SNPdbe	rs730881613
MSV3d	rs730881613
GWAS Ctlg	rs730881613

Max Magnitude

6

ClinVar
Risk	rs730881613(-;-)
Alt	rs730881613(-;-)
Reference	Rs730881613(C;C)
Significance	Pathogenic
Disease	Familial cancer of breast Breast-ovarian cancer
Variation	info
Gene	BRCA2
CLNDBN	Familial cancer of breast Breast-ovarian cancer, familial 2
Reversed	0
HGVS	NC_000013.10:g.32930717delC
CLNSRC
CLNACC	RCV000160305.1, RCV000241442.1,