rs886059573 Rat Genome Database

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Variant: rs886059573 -  Homo sapiens

RGD ID: 11659668
RS ID: rs886059573
ClinVar ID: CV294039
Genic Status: INTERGENIC
Type: SNV (SO:0001483) 
Reference Nucleotide: T
Variant Nucleotide: C
Position
Assembly Chr Position
GRCh37 4 68,620,975
GRCh38 4 67,755,257
JBrowse: View Region in Genome Browser (JBrowse)
Model



HGVS Name(s)
Last Evaluated
Molecular Consequence
Clinical Significance
Trait Synonyms
NG_009293.1:g.5830A>G
NC_000004.12:g.67755257T>C
NC_000004.11:g.68620975T>C
NM_000406.2:c.-922A>G
More... 		01/13/2018 5 prime utr variant uncertain significance HYPOGONADOTROPIC HYPOGONADISM 7 WITHOUT ANOSMIA
Object Symbol
Species
Term
Qualifier
Evidence
With
Reference
Notes
Source
Original Reference(s)
CV294039Humanhypogonadotropic hypogonadism 7 with or without anosmia  IAGP 8554872ClinVar Annotator: match by term: Hypogonadotropic hypogonadism 7 with or without anosmiaClinVar 


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Database
Acc Id
Source(s)
ClinVar RCV000360097 CLINVAR
dbSNP (RS) rs886059573 CLINVAR
MedGen C0342384 CLINVAR
NCBI Gene GNRHR CLINVAR
OMIM 138850 CLINVAR
  146110 CLINVAR