RGD:11595985 Rat Genome Database

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Variant: RGD:11595985 -  Homo sapiens

RGD ID: 11595985
RS ID: rs61375018
ClinVar ID: CV299454
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: ALB  
Reference Nucleotide: T
Variant Nucleotide: C
Position
Assembly Chr Position
GRCh37 4 74,276,026
GRCh38 4 73,410,309
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NG_009291.1:g.11055T>C
NC_000004.12:g.73410309T>C
NC_000004.11:g.74276026T>C
NM_000477.5:c.616-3T>C
More... 		10/01/2023 intron variant benign|uncertain significance EUTHYROID HYPERTHYROXINEMIA 1; none provided
Disease Annotations     Click to see Annotation Detail View


Variant Details
Variant Transcripts
Gene Symbol:ALB
Accession:NM_000477
Location:INTRON

Variant Samples
Additional References at PubMed
PMID:28492532  


Additional Information

Database Acc Id Source(s)
ClinVar RCV000376974 CLINVAR
  RCV000957568 CLINVAR
dbSNP (RS) rs61375018 CLINVAR
MedGen C0342185 CLINVAR
  C3661900 CLINVAR
NCBI Gene ALB CLINVAR
OMIM 103600 CLINVAR
  615999 CLINVAR