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rs41293469

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs41293469(C;T)
Make rs41293469(T;T)
ReferenceGRCh38 38.1/141
Chromosome13
Position32326502
GeneBRCA2
is asnp
is mentioned by
dbSNPrs41293469
ebirs41293469
HLIrs41293469
Exacrs41293469
Varsomers41293469
Maprs41293469
PheGenIrs41293469
hapmaprs41293469
1000 genomesrs41293469
hgdprs41293469
ensemblrs41293469
gopubmedrs41293469
geneviewrs41293469
scholarrs41293469
googlers41293469
pharmgkbrs41293469
gwascentralrs41293469
openSNPrs41293469
23andMers41293469
23andMe allrs41293469
SNP Nexus

SNPshotrs41293469
SNPdbers41293469
MSV3drs41293469
GWAS Ctlgrs41293469
Max Magnitude0
ClinVar
Risk rs41293469(T;T)
Alt rs41293469(T;T)
Reference rs41293469(C;C)
Significance Untested
Disease Hereditary breast and ovarian cancer syndrome Breast-ovarian cancer Hereditary cancer-predisposing syndrome not specified
Variation info
Gene BRCA2
CLNDBN Hereditary breast and ovarian cancer syndrome Breast-ovarian cancer, familial 2 Hereditary cancer-predisposing syndrome not specified
Reversed 0
HGVS NC_000013.10:g.32900639C>T
CLNSRC Ambry Genetics ClinVar
CLNACC RCV000044608.3, RCV000083113.2, RCV000132017.2, RCV000217766.1,