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rs398122669

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs398122669(-;-)
Make rs398122669(-;T)
ReferenceGRCh38 38.1/141
Chromosome17
Position43092757
GeneBRCA1
is asnp
is mentioned by
dbSNPrs398122669
ebirs398122669
HLIrs398122669
Exacrs398122669
Varsomers398122669
Maprs398122669
PheGenIrs398122669
hapmaprs398122669
1000 genomesrs398122669
hgdprs398122669
ensemblrs398122669
gopubmedrs398122669
geneviewrs398122669
scholarrs398122669
googlers398122669
pharmgkbrs398122669
gwascentralrs398122669
openSNPrs398122669
23andMers398122669
23andMe allrs398122669
SNP Nexus

SNPshotrs398122669
SNPdbers398122669
MSV3drs398122669
GWAS Ctlgrs398122669
Max Magnitude0
ClinVar
Risk rs398122669(;)
Alt rs398122669(;)
Reference rs398122669(T;T)
Significance Pathogenic
Disease Breast-ovarian cancer
Variation info
Gene BRCA1
CLNDBN Breast-ovarian cancer, familial 1
Reversed 1
HGVS NC_000017.10:g.41244774delA
CLNSRC ClinVar
CLNACC RCV000077118.2,