rs864622134

Orientation

plus

Stabilized

plus

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

Make rs864622134(-;-)

Reference

GRCh38.p2 38.2/146

Chromosome

13

Position

32338004

Gene

BRCA2

is a	snp
is	mentioned by
dbSNP	rs864622134
dbSNP (classic)	rs864622134
ClinGen	rs864622134
ebi	rs864622134
HLI	rs864622134
Exac	rs864622134
Gnomad	rs864622134
Varsome	rs864622134
LitVar	rs864622134
Map	rs864622134
PheGenI	rs864622134
Biobank	rs864622134
1000 genomes	rs864622134
hgdp	rs864622134
ensembl	rs864622134
geneview	rs864622134
scholar	rs864622134
google	rs864622134
pharmgkb	rs864622134
gwascentral	rs864622134
openSNP	rs864622134
23andMe	rs864622134
SNPshot	rs864622134
SNPdbe	rs864622134
MSV3d	rs864622134
GWAS Ctlg	rs864622134

Max Magnitude

6

ClinVar
Risk	rs864622134(-;-)
Alt	rs864622134(-;-)
Reference	Rs864622134(A;A)
Significance	Pathogenic
Disease	Hereditary breast and ovarian cancer syndrome Breast-ovarian cancer
Variation	info
Gene	BRCA2
CLNDBN	Hereditary breast and ovarian cancer syndrome Breast-ovarian cancer, familial 2
Reversed	0
HGVS	NC_000013.10:g.32912141delA
CLNSRC
CLNACC	RCV000203787.1, RCV000240988.1,