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rs398122653

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(AA;AA) 0 common in clinvar
Make rs398122653(-;-)
Make rs398122653(-;AA)
ReferenceGRCh38 38.1/141
Chromosome17
Position43093399
GeneBRCA1
is asnp
is mentioned by
dbSNPrs398122653
ebirs398122653
HLIrs398122653
Exacrs398122653
Varsomers398122653
Maprs398122653
PheGenIrs398122653
hapmaprs398122653
1000 genomesrs398122653
hgdprs398122653
ensemblrs398122653
gopubmedrs398122653
geneviewrs398122653
scholarrs398122653
googlers398122653
pharmgkbrs398122653
gwascentralrs398122653
openSNPrs398122653
23andMers398122653
23andMe allrs398122653
SNP Nexus

SNPshotrs398122653
SNPdbers398122653
MSV3drs398122653
GWAS Ctlgrs398122653
Max Magnitude0
ClinVar
Risk rs398122653(;)
Alt rs398122653(;)
Reference rs398122653(AA;AA)
Significance Pathogenic
Disease Breast-ovarian cancer Hereditary cancer-predisposing syndrome
Variation info
Gene BRCA1
CLNDBN Breast-ovarian cancer, familial 1 Hereditary cancer-predisposing syndrome
Reversed 1
HGVS NC_000017.10:g.41245416_41245417delTT
CLNSRC ClinVar
CLNACC RCV000077094.2, RCV000164437.1,