RGD:28902500 Rat Genome Database

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Variant: RGD:28902500 -  Homo sapiens

RGD ID: 28902500
RS ID: rs1231172432
ClinVar ID: CV892076
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: GNRHR  
Reference Nucleotide: A
Variant Nucleotide: G
Position
Assembly Chr Position
GRCh37 4 68,603,954
GRCh38 4 67,738,236
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_000406.3:c.*2244T>C
NM_001012763.2:c.*2353T>C
NG_009293.1:g.22851T>C
NC_000004.12:g.67738236A>G
More... 		01/13/2018 3 prime utr variant uncertain significance HYPOGONADOTROPIC HYPOGONADISM 7 WITHOUT ANOSMIA
Disease Annotations     Click to see Annotation Detail View


Variant Details
Variant Transcripts
Gene Symbol:GNRHR
Accession:NM_001012763
Location:3UTRS;EXON

Gene Symbol:GNRHR
Accession:NM_000406
Location:3UTRS;EXON

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV001157146 CLINVAR
dbSNP (RS) rs1231172432 CLINVAR
MedGen C0342384 CLINVAR
NCBI Gene GNRHR CLINVAR
OMIM 138850 CLINVAR
  146110 CLINVAR