rs786204281

Orientation

plus

Stabilized

plus

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

Make rs786204281(A;A)

Reference

GRCh38.p2 38.2/146

Chromosome

13

Position

32355193

Gene

BRCA2

is a	snp
is	mentioned by
dbSNP	rs786204281
dbSNP (classic)	rs786204281
ClinGen	rs786204281
ebi	rs786204281
HLI	rs786204281
Exac	rs786204281
Gnomad	rs786204281
Varsome	rs786204281
LitVar	rs786204281
Map	rs786204281
PheGenI	rs786204281
Biobank	rs786204281
1000 genomes	rs786204281
hgdp	rs786204281
ensembl	rs786204281
geneview	rs786204281
scholar	rs786204281
google	rs786204281
pharmgkb	rs786204281
gwascentral	rs786204281
openSNP	rs786204281
23andMe	rs786204281
SNPshot	rs786204281
SNPdbe	rs786204281
MSV3d	rs786204281
GWAS Ctlg	rs786204281

Max Magnitude

6

ClinVar
Risk	rs786204281(A;A)
Alt	rs786204281(A;A)
Reference	Rs786204281(-;-)
Significance	Pathogenic
Disease	Breast-ovarian cancer
Variation	info
Gene	BRCA2
CLNDBN	Breast-ovarian cancer, familial 2
Reversed	0
HGVS	NC_000013.10:g.32929330dupA
CLNSRC
CLNACC	RCV000168596.3,