rs151139669 Rat Genome Database

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Variant: rs151139669 -  Homo sapiens

RGD ID: 11588520
RS ID: rs151139669
ClinVar ID: CV295549
Genic Status: GENIC
Type: deletion (SO:0000159) 
Associated Genes: ENAM  
Reference Nucleotide: T
Variant Nucleotide: -
Position
Assembly Chr Position
GRCh37 4 71,512,434
GRCh38 4 70,646,717
JBrowse: View Region in Genome Browser (JBrowse)
Model



HGVS Name(s)
Last Evaluated
Molecular Consequence
Clinical Significance
Trait Synonyms
NM_031889.3:c.*1861del
NG_013024.1:g.22973del
NC_000004.11:g.71512433del
NM_031889.2:c.*1861delT
More... 		06/14/2016 3 prime utr variant likely benign
Object Symbol
Species
Term
Qualifier
Evidence
With
Reference
Notes
Source
Original Reference(s)
CV295549Humanamelogenesis imperfecta type 1B  IAGP 8554872ClinVar Annotator: match by term: Amelogenesis Imperfecta and DominantClinVar 


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Database
Acc Id
Source(s)
ClinVar RCV000303739 CLINVAR
dbSNP (RS) rs151139669 CLINVAR
MedGen CN239159 CLINVAR
NCBI Gene ENAM CLINVAR
OMIM 606585 CLINVAR