RGD:11589064 Rat Genome Database

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Variant: RGD:11589064 -  Homo sapiens

RGD ID: 11589064
RS ID: rs6552113
ClinVar ID: CV299275
Genic Status: INTERGENIC
Type: SNV (SO:0001483) 
Reference Nucleotide: T
Variant Nucleotide: C
Position
Assembly Chr Position
GRCh37 4 68,620,957
GRCh38 4 67,755,239
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.5848A>G
NC_000004.12:g.67755239T>C
NC_000004.11:g.68620957T>C
NM_000406.2:c.-904A>G
More... 		01/12/2018 5 prime utr variant benign|likely benign HYPOGONADOTROPIC HYPOGONADISM 7 WITHOUT ANOSMIA
Disease Annotations     Click to see Annotation Detail View


Variant Details
Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV000307832 CLINVAR
dbSNP (RS) rs6552113 CLINVAR
MedGen C0342384 CLINVAR
NCBI Gene GNRHR CLINVAR
OMIM 138850 CLINVAR
  146110 CLINVAR