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rs9534262

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common/normal
(C;T) 0 benign variant
(T;T) 0 common/normal
ReferenceGRCh38 38.1/141
Chromosome13
Position32362509
GeneBRCA2
is asnp
is mentioned by
dbSNPrs9534262
ebirs9534262
HLIrs9534262
Exacrs9534262
Varsomers9534262
Maprs9534262
PheGenIrs9534262
hapmaprs9534262
1000 genomesrs9534262
hgdprs9534262
ensemblrs9534262
gopubmedrs9534262
geneviewrs9534262
scholarrs9534262
googlers9534262
pharmgkbrs9534262
gwascentralrs9534262
openSNPrs9534262
23andMers9534262
23andMe allrs9534262
SNP Nexus

SNPshotrs9534262
SNPdbers9534262
MSV3drs9534262
GWAS Ctlgrs9534262
Max Magnitude0

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 Familial cancer of breast Hereditary cancer-predisposing syndrome not specified
Variation info
Gene BRCA2
CLNDBN Breast-ovarian cancer, familial 2 Familial cancer of breast Hereditary cancer-predisposing syndrome not specified
Reversed 0
HGVS NC_000013.10:g.32936646T>C
CLNSRC Breast Cancer Information Core (BRCA2) Inc.
CLNACC RCV000113823.3, RCV000124004.2, RCV000132168.2, RCV000152883.3,