rs886059567 Rat Genome Database

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Variant: rs886059567 -  Homo sapiens

RGD ID: 11653357
RS ID: rs886059567
ClinVar ID: CV299278
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: GNRHR  
Reference Nucleotide: T
Variant Nucleotide: C
Position
Assembly Chr Position
GRCh37 4 68,606,451
GRCh38 4 67,740,733
JBrowse: View Region in Genome Browser (JBrowse)
Model



HGVS Name(s)
Last Evaluated
Molecular Consequence
Clinical Significance
Trait Synonyms
NG_009293.1:g.20354A>G
NC_000004.12:g.67740733T>C
NC_000004.11:g.68606451T>C
NM_000406.2:c.743-9A>G
More... 		01/12/2018 intron variant uncertain significance HYPOGONADOTROPIC HYPOGONADISM 7 WITHOUT ANOSMIA
Object Symbol
Species
Term
Qualifier
Evidence
With
Reference
Notes
Source
Original Reference(s)
CV299278Humanhypogonadotropic hypogonadism 7 with or without anosmia  IAGP 8554872ClinVar Annotator: match by term: Hypogonadotropic hypogonadism 7 with or without anosmiaClinVar 
Gene Symbol:GNRHR
Accession:NM_000406
Location:INTRON

Gene Symbol:GNRHR
Accession:NM_001012763
Location:INTRON

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Database
Acc Id
Source(s)
ClinVar RCV000310316 CLINVAR
dbSNP (RS) rs886059567 CLINVAR
MedGen C0342384 CLINVAR
NCBI Gene GNRHR CLINVAR
OMIM 138850 CLINVAR
  146110 CLINVAR