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rs398122648

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(;) 0 common in clinvar
Make rs398122648(-;-)
Make rs398122648(-;G)
Make rs398122648(G;G)
ReferenceGRCh38 38.1/141
Chromosome17
Position43124078
GeneBRCA1, NBR2
is asnp
is mentioned by
dbSNPrs398122648
ebirs398122648
HLIrs398122648
Exacrs398122648
Varsomers398122648
Maprs398122648
PheGenIrs398122648
hapmaprs398122648
1000 genomesrs398122648
hgdprs398122648
ensemblrs398122648
gopubmedrs398122648
geneviewrs398122648
scholarrs398122648
googlers398122648
pharmgkbrs398122648
gwascentralrs398122648
openSNPrs398122648
23andMers398122648
23andMe allrs398122648
SNP Nexus

SNPshotrs398122648
SNPdbers398122648
MSV3drs398122648
GWAS Ctlgrs398122648
Max Magnitude0
ClinVar
Risk rs398122648(G;G)
Alt rs398122648(G;G)
Reference rs398122648(;)
Significance Pathogenic
Disease Breast-ovarian cancer
Variation info
Gene NBR2 BRCA1
CLNDBN Breast-ovarian cancer, familial 1
Reversed 1
HGVS NC_000017.10:g.41276095_41276096insC
CLNSRC ClinVar
CLNACC RCV000077086.2,