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rs398122769

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(-;-) 0 common in clinvar
Make rs398122769(-;A)
Make rs398122769(A;A)
ReferenceGRCh38 38.1/141
Chromosome13
Position32338063
GeneBRCA2
is asnp
is mentioned by
dbSNPrs398122769
ClinGenrs398122769
ebirs398122769
HLIrs398122769
Exacrs398122769
Varsomers398122769
Maprs398122769
PheGenIrs398122769
hapmaprs398122769
1000 genomesrs398122769
hgdprs398122769
ensemblrs398122769
gopubmedrs398122769
geneviewrs398122769
scholarrs398122769
googlers398122769
pharmgkbrs398122769
gwascentralrs398122769
openSNPrs398122769
23andMers398122769
23andMe allrs398122769
SNP Nexus

SNPshotrs398122769
SNPdbers398122769
MSV3drs398122769
GWAS Ctlgrs398122769
Max Magnitude0
ClinVar
Risk rs398122769(A;A)
Alt rs398122769(A;A)
Reference Rs398122769(;)
Significance Pathogenic
Disease Breast-ovarian cancer Familial cancer of breast
Variation info
Gene BRCA2
CLNDBN Breast-ovarian cancer, familial 2 Familial cancer of breast
Reversed 0
HGVS NC_000013.10:g.32912200dupA
CLNSRC ClinVar
CLNACC RCV000077713.4, RCV000160278.1,