rs4305020 Rat Genome Database

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Variant: rs4305020 -  Homo sapiens

RGD ID: 14719526
RS ID: rs4305020
ClinVar ID: CV668341
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: LOC130058203  
Reference Nucleotide: C
Variant Nucleotide: G
Position
Assembly Chr Position
GRCh37 16 2,033,970
GRCh38 16 1,983,969
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Clinical Significance Trait Synonyms
NG_016288.1:g.4821C>G
NC_000016.10:g.1983969C>G
NC_000016.9:g.2033970C>G
NM_005262.2:c.-250C>G
More... 		06/19/2018 benign none provided; RECLASSIFIED - ADRA2C POLYMORPHISM; RECLASSIFIED - ADRB1 POLYMORPHISM

Variant Details
Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV000830817 CLINVAR
dbSNP (RS) rs4305020 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene GFER CLINVAR
  LOC130058203 CLINVAR
OMIM 600924 CLINVAR