rs786203537

Orientation

plus

Stabilized

plus

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

Make rs786203537(A;A)

Reference

GRCh38.p2 38.2/146

Chromosome

13

Position

32338191

Gene

BRCA2

is a	snp
is	mentioned by
dbSNP	rs786203537
dbSNP (classic)	rs786203537
ClinGen	rs786203537
ebi	rs786203537
HLI	rs786203537
Exac	rs786203537
Gnomad	rs786203537
Varsome	rs786203537
LitVar	rs786203537
Map	rs786203537
PheGenI	rs786203537
Biobank	rs786203537
1000 genomes	rs786203537
hgdp	rs786203537
ensembl	rs786203537
geneview	rs786203537
scholar	rs786203537
google	rs786203537
pharmgkb	rs786203537
gwascentral	rs786203537
openSNP	rs786203537
23andMe	rs786203537
SNPshot	rs786203537
SNPdbe	rs786203537
MSV3d	rs786203537
GWAS Ctlg	rs786203537

Max Magnitude

6

ClinVar
Risk	rs786203537(A;A)
Alt	rs786203537(A;A)
Reference	Rs786203537(-;-)
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.32912328dupA
CLNSRC
CLNACC	RCV000166888.1, RCV000241488.1,