rs786202756

Orientation

plus

Stabilized

plus

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

Make rs786202756(-;-)

Reference

GRCh38.p2 38.2/146

Chromosome

13

Position

32333333

Gene

BRCA2

is a	snp
is	mentioned by
dbSNP	rs786202756
dbSNP (classic)	rs786202756
ClinGen	rs786202756
ebi	rs786202756
HLI	rs786202756
Exac	rs786202756
Gnomad	rs786202756
Varsome	rs786202756
LitVar	rs786202756
Map	rs786202756
PheGenI	rs786202756
Biobank	rs786202756
1000 genomes	rs786202756
hgdp	rs786202756
ensembl	rs786202756
geneview	rs786202756
scholar	rs786202756
google	rs786202756
pharmgkb	rs786202756
gwascentral	rs786202756
openSNP	rs786202756
23andMe	rs786202756
SNPshot	rs786202756
SNPdbe	rs786202756
MSV3d	rs786202756
GWAS Ctlg	rs786202756

Max Magnitude

6

rs786202756 has merged into rs397507611

ClinVar
Risk	rs786202756(-;-)
Alt	rs786202756(-;-)
Reference	Rs786202756(C;C)
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.32907470delC
CLNSRC
CLNACC	RCV000165730.1, RCV000241106.1,