rs1731942957 Rat Genome Database

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Variant: rs1731942957 -  Homo sapiens

RGD ID: 28899015
RS ID: rs1731942957
ClinVar ID: CV892100
Genic Status: INTERGENIC
Type: SNV (SO:0001483) 
Reference Nucleotide: A
Variant Nucleotide: G
Position
Assembly Chr Position
GRCh37 4 68,620,752
GRCh38 4 67,755,034
JBrowse: View Region in Genome Browser (JBrowse)
Model



HGVS Name(s)
Last Evaluated
Clinical Significance
Trait Synonyms
NC_000004.12:g.67755034A>G
NG_009293.1:g.6053T>C
NC_000004.11:g.68620752A>G
NM_001012763.1:c.-699T>C
More... 		01/13/2018 uncertain significance HYPOGONADOTROPIC HYPOGONADISM 7 WITHOUT ANOSMIA
Object Symbol
Species
Term
Qualifier
Evidence
With
Reference
Notes
Source
Original Reference(s)
CV892100Humanhypogonadotropic 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 RCV001155666 CLINVAR
dbSNP (RS) rs1731942957 CLINVAR
MedGen C0342384 CLINVAR
NCBI Gene GNRHR CLINVAR
OMIM 138850 CLINVAR
  146110 CLINVAR