rs73258136 Rat Genome Database

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Variant: rs73258136 -  Homo sapiens

RGD ID: 14742829
RS ID: rs73258136
ClinVar ID: CV661006
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: LOC129994533  
Reference Nucleotide: T
Variant Nucleotide: C
Position
Assembly Chr Position
GRCh37 5 130,501,074
GRCh38 5 131,165,381
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Clinical Significance Trait Synonyms
NG_032998.1:g.4968A>G
NC_000005.10:g.131165381T>C
NC_000005.9:g.130501074T>C
NM_005340.6:c.-176A>G
More... 		06/16/2018 benign none provided; RECLASSIFIED - ADRA2C POLYMORPHISM; RECLASSIFIED - ADRB1 POLYMORPHISM

Variant Details
Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV000841654 CLINVAR
dbSNP (RS) rs73258136 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene HINT1 CLINVAR
  LOC129994533 CLINVAR
OMIM 601314 CLINVAR