rs786203546

Orientation

plus

Stabilized

plus

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

Make rs786203546(-;-)

Reference

GRCh38.p2 38.2/146

Chromosome

13

Position

32354879

Gene

BRCA2

is a	snp
is	mentioned by
dbSNP	rs786203546
dbSNP (classic)	rs786203546
ClinGen	rs786203546
ebi	rs786203546
HLI	rs786203546
Exac	rs786203546
Gnomad	rs786203546
Varsome	rs786203546
LitVar	rs786203546
Map	rs786203546
PheGenI	rs786203546
Biobank	rs786203546
1000 genomes	rs786203546
hgdp	rs786203546
ensembl	rs786203546
geneview	rs786203546
scholar	rs786203546
google	rs786203546
pharmgkb	rs786203546
gwascentral	rs786203546
openSNP	rs786203546
23andMe	rs786203546
SNPshot	rs786203546
SNPdbe	rs786203546
MSV3d	rs786203546
GWAS Ctlg	rs786203546

Max Magnitude

6

aka c.7026delA

ClinVar
Risk	rs786203546(-;-)
Alt	rs786203546(-;-)
Reference	Rs786203546(A;A)
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.32929016delA
CLNSRC
CLNACC	RCV000166905.1, RCV000241486.1,