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rs41293517

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs41293517(C;T)
Make rs41293517(T;T)
ReferenceGRCh38 38.1/141
Chromosome13
Position32370429
GeneBRCA2
is asnp
is mentioned by
dbSNPrs41293517
ebirs41293517
HLIrs41293517
Exacrs41293517
Varsomers41293517
Maprs41293517
PheGenIrs41293517
hapmaprs41293517
1000 genomesrs41293517
hgdprs41293517
ensemblrs41293517
gopubmedrs41293517
geneviewrs41293517
scholarrs41293517
googlers41293517
pharmgkbrs41293517
gwascentralrs41293517
openSNPrs41293517
23andMers41293517
23andMe allrs41293517
SNP Nexus

SNPshotrs41293517
SNPdbers41293517
MSV3drs41293517
GWAS Ctlgrs41293517
Max Magnitude0
ClinVar
Risk rs41293517(T;T)
Alt rs41293517(T;T)
Reference rs41293517(C;C)
Significance Untested
Disease Familial cancer of breast Breast-ovarian cancer Hereditary cancer-predisposing syndrome
Variation info
Gene BRCA2
CLNDBN Familial cancer of breast Breast-ovarian cancer, familial 2 Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000013.10:g.32944566C>T
CLNSRC Ambry Genetics ClinVar
CLNACC RCV000045491.2, RCV000113912.1, RCV000130122.2,