RGD:407497785 Rat Genome Database

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Variant: RGD:407497785 -  Homo sapiens

RGD ID: 407497785
ClinVar ID: CV3441747
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: EFHB  
Reference Nucleotide: C
Variant Nucleotide: G
Position
Assembly Chr Position
GRCh37 3 19,930,107
GRCh38 3 19,888,615
JBrowse: View Region in Genome Browser (JBrowse)
Model



HGVS Name(s)
Last Evaluated
Molecular Consequence
Clinical Significance
Trait Synonyms
NM_001330688.2:c.1372G>C
NM_144715.4:c.1762G>C
NC_000003.12:g.19888615C>G
NC_000003.11:g.19930107C>G
More... 		05/29/2024 missense variant uncertain significance AllHighlyPenetrant

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Database
Acc Id
Source(s)
ClinVar RCV004622294 CLINVAR
MedGen CN169374 CLINVAR
NCBI Gene EFHB CLINVAR