RGD:596947285 Rat Genome Database

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Variant: RGD:596947285 -  Homo sapiens

RGD ID: 596947285
ClinVar ID: CV3548835
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: SLBP  
Reference Nucleotide: A
Variant Nucleotide: G
Position
Assembly Chr Position
GRCh37 4 1,698,072
GRCh38 4 1,696,345
JBrowse: View Region in Genome Browser (JBrowse)
Model



HGVS Name(s)
Last Evaluated
Molecular Consequence
Clinical Significance
Trait Synonyms
NM_001306075.2:c.369T>C
NM_001306074.2:c.381T>C
NM_006527.4:c.486T>C
NC_000004.12:g.1696345A>G
More... 		09/01/2024 synonymous variant likely benign none provided; RECLASSIFIED - ADRA2C POLYMORPHISM; RECLASSIFIED - ADRB1 POLYMORPHISM

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Database
Acc Id
Source(s)
ClinVar RCV004811159 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene SLBP CLINVAR
OMIM 602422 CLINVAR