rs786202061

Orientation

plus

Stabilized

plus

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

Make rs786202061(-;-)

Reference

GRCh38.p2 38.2/146

Chromosome

13

Position

32340118

Gene

BRCA2

is a	snp
is	mentioned by
dbSNP	rs786202061
dbSNP (classic)	rs786202061
ClinGen	rs786202061
ebi	rs786202061
HLI	rs786202061
Exac	rs786202061
Gnomad	rs786202061
Varsome	rs786202061
LitVar	rs786202061
Map	rs786202061
PheGenI	rs786202061
Biobank	rs786202061
1000 genomes	rs786202061
hgdp	rs786202061
ensembl	rs786202061
geneview	rs786202061
scholar	rs786202061
google	rs786202061
pharmgkb	rs786202061
gwascentral	rs786202061
openSNP	rs786202061
23andMe	rs786202061
SNPshot	rs786202061
SNPdbe	rs786202061
MSV3d	rs786202061
GWAS Ctlg	rs786202061

Max Magnitude

6

ClinVar
Risk	rs786202061(-;-)
Alt	rs786202061(-;-)
Reference	Rs786202061(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.32914255delT
CLNSRC
CLNACC	RCV000164683.1, RCV000241035.1,