rs786202160

Orientation

plus

Stabilized

plus

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

Make rs786202160(-;-)

Reference

GRCh38.p2 38.2/146

Chromosome

13

Position

32337720

Gene

BRCA2

is a	snp
is	mentioned by
dbSNP	rs786202160
dbSNP (classic)	rs786202160
ClinGen	rs786202160
ebi	rs786202160
HLI	rs786202160
Exac	rs786202160
Gnomad	rs786202160
Varsome	rs786202160
LitVar	rs786202160
Map	rs786202160
PheGenI	rs786202160
Biobank	rs786202160
1000 genomes	rs786202160
hgdp	rs786202160
ensembl	rs786202160
geneview	rs786202160
scholar	rs786202160
google	rs786202160
pharmgkb	rs786202160
gwascentral	rs786202160
openSNP	rs786202160
23andMe	rs786202160
SNPshot	rs786202160
SNPdbe	rs786202160
MSV3d	rs786202160
GWAS Ctlg	rs786202160

Max Magnitude

6

ClinVar
Risk	rs786202160(-;-)
Alt	rs786202160(-;-)
Reference	Rs786202160(G;G)
Significance	Pathogenic
Disease	Hereditary cancer-predisposing syndrome Breast-ovarian cancer not provided
Variation	info
Gene	BRCA2
CLNDBN	Hereditary cancer-predisposing syndrome Breast-ovarian cancer, familial 2 not provided
Reversed	0
HGVS	NC_000013.10:g.32911857delG
CLNSRC
CLNACC	RCV000164839.1, RCV000241513.1, RCV000482439.1,