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rs398122561

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs398122561(A;T)
Make rs398122561(T;T)
ReferenceGRCh38 38.1/141
Chromosome13
Position32340941
GeneBRCA2
is asnp
is mentioned by
dbSNPrs398122561
ebirs398122561
HLIrs398122561
Exacrs398122561
Varsomers398122561
Maprs398122561
PheGenIrs398122561
hapmaprs398122561
1000 genomesrs398122561
hgdprs398122561
ensemblrs398122561
gopubmedrs398122561
geneviewrs398122561
scholarrs398122561
googlers398122561
pharmgkbrs398122561
gwascentralrs398122561
openSNPrs398122561
23andMers398122561
23andMe allrs398122561
SNP Nexus

SNPshotrs398122561
SNPdbers398122561
MSV3drs398122561
GWAS Ctlgrs398122561
Max Magnitude0
ClinVar
Risk rs398122561(T;T)
Alt rs398122561(T;T)
Reference rs398122561(A;A)
Significance Pathogenic
Disease Breast-ovarian cancer
Variation info
Gene BRCA2
CLNDBN Breast-ovarian cancer, familial 2
Reversed 0
HGVS NC_000013.10:g.32915078A>T
CLNSRC ClinVar
CLNACC RCV000076970.2,