rs786203575

Orientation

plus

Stabilized

plus

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

Make rs786203575(-;-)

Reference

GRCh38.p2 38.2/146

Chromosome

13

Position

32379821

Gene

BRCA2

is a	snp
is	mentioned by
dbSNP	rs786203575
dbSNP (classic)	rs786203575
ClinGen	rs786203575
ebi	rs786203575
HLI	rs786203575
Exac	rs786203575
Gnomad	rs786203575
Varsome	rs786203575
LitVar	rs786203575
Map	rs786203575
PheGenI	rs786203575
Biobank	rs786203575
1000 genomes	rs786203575
hgdp	rs786203575
ensembl	rs786203575
geneview	rs786203575
scholar	rs786203575
google	rs786203575
pharmgkb	rs786203575
gwascentral	rs786203575
openSNP	rs786203575
23andMe	rs786203575
SNPshot	rs786203575
SNPdbe	rs786203575
MSV3d	rs786203575
GWAS Ctlg	rs786203575

Max Magnitude

6

ClinVar
Risk	rs786203575(-;-)
Alt	rs786203575(-;-)
Reference	Rs786203575(T;T)
Significance	Pathogenic
Disease	Hereditary cancer-predisposing syndrome Breast-ovarian cancer
Variation	info
Gene	BRCA2
CLNDBN	Hereditary cancer-predisposing syndrome Breast-ovarian cancer, familial 2
Reversed	0
HGVS	NC_000013.10:g.32953958delT
CLNSRC
CLNACC	RCV000166953.1, RCV000241186.2,