RGD:151797230 Rat Genome Database

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Variant: RGD:151797230 -  Homo sapiens

RGD ID: 151797230
RS ID: rs374350459
ClinVar ID: CV1401115
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: GHRHR  
Reference Nucleotide: G
Variant Nucleotide: A
Position
Assembly Chr Position
GRCh37 7 31,016,940
GRCh38 7 30,977,325
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_000823.4:c.1146+3G>A
NG_021416.1:g.18305G>A
NC_000007.14:g.30977325G>A
NC_000007.13:g.31016940G>A
 05/18/2021 intron variant uncertain significance none provided

Variant Details
Variant Transcripts
Gene Symbol:GHRHR
Accession:NM_000823
Location:INTRON

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


Additional Information

Database Acc Id Source(s)
ClinVar RCV002011240 CLINVAR
dbSNP (RS) rs374350459 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene GHRHR CLINVAR
OMIM 139191 CLINVAR