rs9534262

plus

Geno	Mag	Summary
(C;C)	0	common/normal
(C;T)	0	benign variant
(T;T)	0	common/normal

Reference

GRCh38 38.1/141

Chromosome

13

Position

32362509

Gene

BRCA2

is a	snp
is	mentioned by
dbSNP	rs9534262
dbSNP (classic)	rs9534262
ClinGen	rs9534262
ebi	rs9534262
HLI	rs9534262
Exac	rs9534262
Gnomad	rs9534262
Varsome	rs9534262
LitVar	rs9534262
Map	rs9534262
PheGenI	rs9534262
Biobank	rs9534262
1000 genomes	rs9534262
hgdp	rs9534262
ensembl	rs9534262
geneview	rs9534262
scholar	rs9534262
google	rs9534262
pharmgkb	rs9534262
gwascentral	rs9534262
openSNP	rs9534262
23andMe	rs9534262
SNPshot	rs9534262
SNPdbe	rs9534262
MSV3d	rs9534262
GWAS Ctlg	rs9534262

Max Magnitude

0

rs9534262, also known as c.7806-14T>C, is a variant in the BRCA2 gene classified as benign by multiple ClinVar submitters.

?

(C;C) (C;T) (T;T)

28

[PMID 24123850] Capillary electrophoresis analysis of conventional splicing assays: IARC analytical and clinical classification of 31 BRCA2 genetic variants

ClinVar
Risk	Rs9534262(C;C)
Alt	Rs9534262(C;C)
Reference	Rs9534262(T;T)
Significance	Non-pathogenic
Disease	Breast-ovarian cancer Hereditary cancer-predisposing syndrome not specified Hereditary breast and ovarian cancer syndrome Fanconi anemia Familial cancer of breast
Variation	info
Gene	BRCA2
CLNDBN	Breast-ovarian cancer, familial 2 Hereditary cancer-predisposing syndrome not specified Hereditary breast and ovarian cancer syndrome Fanconi anemia Familial cancer of breast
Reversed	0
HGVS	NC_000013.10:g.32936646T>C
CLNSRC	Breast Cancer Information Core (BRCA2)
CLNACC	RCV000113823.3, RCV000132168.2, RCV000152883.5, RCV000331967.2, RCV000386451.1, RCV000459462.1,