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rs387907575

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs387907575(G;T)
Make rs387907575(T;T)
ReferenceGRCh38 38.1/141
Chromosome13
Position32340316
GeneBRCA2
is asnp
is mentioned by
dbSNPrs387907575
ebirs387907575
HLIrs387907575
Exacrs387907575
Varsomers387907575
Maprs387907575
PheGenIrs387907575
hapmaprs387907575
1000 genomesrs387907575
hgdprs387907575
ensemblrs387907575
gopubmedrs387907575
geneviewrs387907575
scholarrs387907575
googlers387907575
pharmgkbrs387907575
gwascentralrs387907575
openSNPrs387907575
23andMers387907575
23andMe allrs387907575
SNP Nexus

SNPshotrs387907575
SNPdbers387907575
MSV3drs387907575
GWAS Ctlgrs387907575
Max Magnitude0
ClinVar
Risk rs387907575(T;T)
Alt rs387907575(T;T)
Reference rs387907575(G;G)
Significance Probable-Pathogenic
Disease Breast-ovarian cancer
Variation info
Gene BRCA2
CLNDBN Breast-ovarian cancer, familial 2
Reversed 0
HGVS NC_000013.10:g.32914453G>T
CLNSRC ClinVar
CLNACC RCV000049344.1,