rs66657532 Rat Genome Database

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Variant: rs66657532 -  Homo sapiens

RGD ID: 14713337
RS ID: rs66657532
ClinVar ID: CV664045
Genic Status: GENIC
Type: deletion (SO:0000159) 
Associated Genes: COL5A1  LOC101448202  
Reference Nucleotide: G
Variant Nucleotide: -
Position
Assembly Chr Position
GRCh37 9 137,714,567
GRCh38 9 134,822,721
JBrowse: View Region in Genome Browser (JBrowse)
Model



HGVS Name(s)
Last Evaluated
Molecular Consequence
Clinical Significance
Trait Synonyms
NM_000093.5:c.4609-278del
NM_001278074.1:c.4609-278del
NG_008030.1:g.185915del
NC_000009.12:g.134822720del
More... 		06/14/2018 intron variant benign none provided

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Database
Acc Id
Source(s)
ClinVar RCV000828688 CLINVAR
dbSNP (RS) rs66657532 CLINVAR
MedGen CN517202 CLINVAR
NCBI Gene 101448202 CLINVAR
  COL5A1 CLINVAR
OMIM 120215 CLINVAR