rs786204278

Orientation

plus

Stabilized

plus

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

Make rs786204278(-;-)

Reference

GRCh38.p2 38.2/146

Chromosome

13

Position

32340529

Gene

BRCA2

is a	snp
is	mentioned by
dbSNP	rs786204278
dbSNP (classic)	rs786204278
ClinGen	rs786204278
ebi	rs786204278
HLI	rs786204278
Exac	rs786204278
Gnomad	rs786204278
Varsome	rs786204278
LitVar	rs786204278
Map	rs786204278
PheGenI	rs786204278
Biobank	rs786204278
1000 genomes	rs786204278
hgdp	rs786204278
ensembl	rs786204278
geneview	rs786204278
scholar	rs786204278
google	rs786204278
pharmgkb	rs786204278
gwascentral	rs786204278
openSNP	rs786204278
23andMe	rs786204278
SNPshot	rs786204278
SNPdbe	rs786204278
MSV3d	rs786204278
GWAS Ctlg	rs786204278

Max Magnitude

6

ClinVar
Risk	rs786204278(-;-)
Alt	rs786204278(-;-)
Reference	Rs786204278(T;T)
Significance	Pathogenic
Disease	Breast-ovarian cancer
Variation	info
Gene	BRCA2
CLNDBN	Breast-ovarian cancer, familial 2
Reversed	0
HGVS	NC_000013.10:g.32914666delT
CLNSRC
CLNACC	RCV000168588.3,