rs786202796

Orientation

plus

Stabilized

plus

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

Make rs786202796(T;T)

Reference

GRCh38.p2 38.2/146

Chromosome

13

Position

32332277

Gene

BRCA2

is a	snp
is	mentioned by
dbSNP	rs786202796
dbSNP (classic)	rs786202796
ClinGen	rs786202796
ebi	rs786202796
HLI	rs786202796
Exac	rs786202796
Gnomad	rs786202796
Varsome	rs786202796
LitVar	rs786202796
Map	rs786202796
PheGenI	rs786202796
Biobank	rs786202796
1000 genomes	rs786202796
hgdp	rs786202796
ensembl	rs786202796
geneview	rs786202796
scholar	rs786202796
google	rs786202796
pharmgkb	rs786202796
gwascentral	rs786202796
openSNP	rs786202796
23andMe	rs786202796
SNPshot	rs786202796
SNPdbe	rs786202796
MSV3d	rs786202796
GWAS Ctlg	rs786202796

Max Magnitude

6

BRCA2 variant known as c.799G>T, p.Gly267Ter, G267X and G267*

ClinVar
Risk	rs786202796(T;T)
Alt	rs786202796(T;T)
Reference	Rs786202796(G;G)
Significance	Pathogenic
Disease	Hereditary cancer-predisposing syndrome not provided Breast-ovarian cancer
Variation	info
Gene	BRCA2
CLNDBN	Hereditary cancer-predisposing syndrome not provided Breast-ovarian cancer, familial 2
Reversed	0
HGVS	NC_000013.10:g.32906414G>T
CLNSRC
CLNACC	RCV000165786.2, RCV000220294.1, RCV000241277.1,