RGD:26898733 Rat Genome Database

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Variant: RGD:26898733 -  Homo sapiens

RGD ID: 26898733
RS ID: rs369437104
ClinVar ID: CV851452
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: IMPG2  
Reference Nucleotide: G
Variant Nucleotide: A
Position
Assembly Chr Position
GRCh37 3 100,972,628
GRCh38 3 101,253,784
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_016247.4:c.1154-3C>T
NG_028284.1:g.71792C>T
NC_000003.12:g.101253784G>A
NC_000003.11:g.100972628G>A
More... 		12/31/2019 intron variant likely benign|uncertain significance none provided

Variant Details
Variant Transcripts
Gene Symbol:IMPG2
Accession:NM_016247
Location:INTRON

Variant Samples
Additional References at PubMed
PMID:9536098   PMID:17576681   PMID:25741868   PMID:28492532  


Additional Information

Database Acc Id Source(s)
ClinVar RCV001066675 CLINVAR
  RCV003953453 CLINVAR
dbSNP (RS) rs369437104 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene IMPG2 CLINVAR
OMIM 607056 CLINVAR