RGD:11663116 Rat Genome Database

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Variant: RGD:11663116 -  Homo sapiens

RGD ID: 11663116
RS ID: rs886059570
ClinVar ID: CV299274
Genic Status: INTERGENIC
Type: SNV (SO:0001483) 
Reference Nucleotide: A
Variant Nucleotide: C
Position
Assembly Chr Position
GRCh37 4 68,620,736
GRCh38 4 67,755,018
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NG_009293.1:g.6069T>G
NC_000004.12:g.67755018A>C
NC_000004.11:g.68620736A>C
NM_001012763.1:c.-683T>G
More...
06/14/2016 5 prime utr variant uncertain significance
Disease Annotations     Click to see Annotation Detail View


Variant Details
Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV000392502 CLINVAR
dbSNP (RS) rs886059570 CLINVAR
MedGen CN239347 CLINVAR
NCBI Gene GNRHR CLINVAR
OMIM 138850 CLINVAR