rs797044450 Rat Genome Database

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Variant: rs797044450 -  Homo sapiens

RGD ID: 13520486
RS ID: rs797044450
ClinVar ID: CV495849
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: GH-LCR  GH1  
Reference Nucleotide: A
Variant Nucleotide: C
Position
Assembly Chr Position
GRCh37 17 61,995,371
GRCh38 17 63,918,011
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NG_011676.1:g.5828T>G
NC_000017.11:g.63918011A>C
NC_000017.10:g.61995371A>C
NM_000515.3:c.291+6T>G
More... 		03/12/2018 intron variant pathogenic none provided

Variant Details
Variant Transcripts
Gene Symbol:GH1
Accession:NM_022559
Location:INTRON

Gene Symbol:GH1
Accession:NM_022560
Location:INTRON

Gene Symbol:GH1
Accession:NM_000515
Location:INTRON

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV000598671 CLINVAR
dbSNP (RS) rs797044450 CLINVAR
MedGen CN517202 CLINVAR
NCBI Gene 106128904 CLINVAR
  GH1 CLINVAR
OMIM 139250 CLINVAR