RGD:156207966 Rat Genome Database

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Variant: RGD:156207966 -  Homo sapiens

RGD ID: 156207966
ClinVar ID: CV2165107
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: NEFH  
Reference Nucleotide: T
Variant Nucleotide: A
Position
Assembly Chr Position
GRCh37 22 29,881,856
GRCh38 22 29,485,867
JBrowse: View Region in Genome Browser (JBrowse)
Model



HGVS Name(s)
Last Evaluated
Molecular Consequence
Clinical Significance
Trait Synonyms
NM_021076.4:c.1208+20T>A
NG_008404.1:g.10676T>A
NC_000022.11:g.29485867T>A
NC_000022.10:g.29881856T>A
 03/24/2022 intron variant likely benign none provided; RECLASSIFIED - ADRA2C POLYMORPHISM; RECLASSIFIED - ADRB1 POLYMORPHISM

Gene Symbol:NEFH
Accession:NM_021076
Location:INTRON

Gene Symbol:NEFH
Accession:XM_011530200
Location:INTRON

.
PMID:28492532  



Database
Acc Id
Source(s)
ClinVar RCV003024697 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene NEFH CLINVAR
OMIM 162230 CLINVAR