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rs398122571

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(AAAG;AAAG) 0 common in clinvar
Make rs398122571(-;-)
Make rs398122571(-;AAAG)
ReferenceGRCh38 38.1/141
Chromosome13
Position32346835
GeneBRCA2
is asnp
is mentioned by
dbSNPrs398122571
ebirs398122571
HLIrs398122571
Exacrs398122571
Varsomers398122571
Maprs398122571
PheGenIrs398122571
hapmaprs398122571
1000 genomesrs398122571
hgdprs398122571
ensemblrs398122571
gopubmedrs398122571
geneviewrs398122571
scholarrs398122571
googlers398122571
pharmgkbrs398122571
gwascentralrs398122571
openSNPrs398122571
23andMers398122571
23andMe allrs398122571
SNP Nexus

SNPshotrs398122571
SNPdbers398122571
MSV3drs398122571
GWAS Ctlgrs398122571
Max Magnitude0
ClinVar
Risk rs398122571(;)
Alt rs398122571(;)
Reference rs398122571(AAAG;AAAG)
Significance Pathogenic
Disease Breast-ovarian cancer
Variation info
Gene BRCA2
CLNDBN Breast-ovarian cancer, familial 2
Reversed 0
HGVS NC_000013.10:g.32920972_32920975delAAAG
CLNSRC ClinVar
CLNACC RCV000076981.2,