RGD:152120410 Rat Genome Database

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Variant: RGD:152120410 -  Homo sapiens

RGD ID: 152120410
RS ID: rs747272834
ClinVar ID: CV1574225
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: GHRHR  LOC129661958  
Reference Nucleotide: G
Variant Nucleotide: C
Position
Assembly Chr Position
GRCh37 7 31,014,667
GRCh38 7 30,975,052
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.882+12G>C
NG_021416.1:g.16032G>C
NC_000007.14:g.30975052G>C
NC_000007.13:g.31014667G>C
 07/28/2021 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 RCV002175498 CLINVAR
dbSNP (RS) rs747272834 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene GHRHR CLINVAR
OMIM 139191 CLINVAR