RGD:11649532 Rat Genome Database

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Variant: RGD:11649532 -  Homo sapiens

RGD ID: 11649532
RS ID: rs886052784
ClinVar ID: CV337797
Genic Status: GENIC
Type: deletion (SO:0000159) 
Associated Genes: LOC110806262  
Reference Nucleotide: G
Variant Nucleotide: -
Position
Assembly Chr Position
GRCh37 17 28,562,910
GRCh38 17 30,235,892
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NG_011747.2:g.5045del
NG_055470.1:g.515del
NM_001045.5:c.-503delC
NC_000017.10:g.28562913del
More... 		06/14/2016 5 prime utr variant uncertain significance behavioral disorder
Disease Annotations     Click to see Annotation Detail View


Variant Details
Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV000287842 CLINVAR
dbSNP (RS) rs886052784 CLINVAR
MedGen C0004930 CLINVAR
NCBI Gene 110806262 CLINVAR
  SLC6A4 CLINVAR
OMIM 182138 CLINVAR