RGD:152109230 Rat Genome Database

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Variant: RGD:152109230 -  Homo sapiens

RGD ID: 152109230
RS ID: rs749787094
ClinVar ID: CV1563842
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: GHRHR  
Reference Nucleotide: C
Variant Nucleotide: T
Position
Assembly Chr Position
GRCh37 7 31,014,111
GRCh38 7 30,974,496
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.812+7C>T
NG_021416.1:g.15476C>T
NC_000007.14:g.30974496C>T
NC_000007.13:g.31014111C>T
 11/10/2021 intron variant likely benign none provided

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

Variant Samples
Additional References at PubMed
PMID:28492532  


Additional Information

Database Acc Id Source(s)
ClinVar RCV002174117 CLINVAR
dbSNP (RS) rs749787094 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene GHRHR CLINVAR
OMIM 139191 CLINVAR