rs786202875

Orientation

plus

Stabilized

plus

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

Make rs786202875(T;T)

Reference

GRCh38.p2 38.2/146

Chromosome

13

Position

32336849

Gene

BRCA2

is a	snp
is	mentioned by
dbSNP	rs786202875
dbSNP (classic)	rs786202875
ClinGen	rs786202875
ebi	rs786202875
HLI	rs786202875
Exac	rs786202875
Gnomad	rs786202875
Varsome	rs786202875
LitVar	rs786202875
Map	rs786202875
PheGenI	rs786202875
Biobank	rs786202875
1000 genomes	rs786202875
hgdp	rs786202875
ensembl	rs786202875
geneview	rs786202875
scholar	rs786202875
google	rs786202875
pharmgkb	rs786202875
gwascentral	rs786202875
openSNP	rs786202875
23andMe	rs786202875
SNPshot	rs786202875
SNPdbe	rs786202875
MSV3d	rs786202875
GWAS Ctlg	rs786202875

Max Magnitude

6

ClinVar
Risk	rs786202875(T;T)
Alt	rs786202875(T;T)
Reference	Rs786202875(G;G)
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.32910986G>T
CLNSRC
CLNACC	RCV000165924.1, RCV000241463.1,