RGD:11608267 Rat Genome Database

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Variant: RGD:11608267 -  Homo sapiens

RGD ID: 11608267
RS ID: rs765427927
ClinVar ID: CV305011
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: GNRH1  
Reference Nucleotide: A
Variant Nucleotide: G
Position
Assembly Chr Position
GRCh37 8 25,280,876
GRCh38 8 25,423,360
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_000825.3:c.-18T>C
NG_016457.1:g.6681T>C
NC_000008.11:g.25423360A>G
NC_000008.10:g.25280876A>G
More... 		06/14/2016 5 prime utr variant uncertain significance
Disease Annotations     Click to see Annotation Detail View


Variant Details
Variant Transcripts
Gene Symbol:GNRH1
Accession:NM_000825
Location:5UTRS;EXON

Gene Symbol:GNRH1
Accession:NM_001083111
Location:5UTRS;INTRON

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV000352875 CLINVAR
dbSNP (RS) rs765427927 CLINVAR
MedGen CN239347 CLINVAR
NCBI Gene GNRH1 CLINVAR
OMIM 152760 CLINVAR