RGD:28895332 Rat Genome Database

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Variant: RGD:28895332 -  Homo sapiens

RGD ID: 28895332
RS ID: rs544836312
ClinVar ID: CV887214
Genic Status: INTERGENIC
Type: SNV (SO:0001483) 
Reference Nucleotide: G
Variant Nucleotide: A
Position
Assembly Chr Position
GRCh37 22 18,560,692
GRCh38 22 18,077,926
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Clinical Significance Trait Synonyms
NC_000022.10:g.18560692G>A
NC_000022.11:g.18077926G>A
NG_008339.1:g.5007G>A
NM_001199319.1:c.-203G>A
More... 		01/15/2018 uncertain significance Peroxisome biogenesis disorder 7A
Disease Annotations     Click to see Annotation Detail View


Variant Details
Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV001140834 CLINVAR
dbSNP (RS) rs544836312 CLINVAR
MedGen C3888385 CLINVAR
NCBI Gene PEX26 CLINVAR
OMIM 608666 CLINVAR
  614872 CLINVAR