RGD:405064187 Rat Genome Database

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Variant: RGD:405064187 -  Homo sapiens

RGD ID: 405064187
ClinVar ID: CV2854865
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: COL3A1  MIR3606  
Reference Nucleotide: T
Variant Nucleotide: C
Position
Assembly Chr Position
GRCh37 2 189,860,406
GRCh38 2 188,995,680
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_000090.4:c.1510-12T>C
LRG_3:g.26308T>C
NG_007404.1:g.26308T>C
NC_000002.12:g.188995680T>C
More... 		12/30/2023 intron variant likely benign Ehlers Danlos syndrome, arterial type; Ehlers Danlos syndrome, ecchymotic type; Ehlers Danlos syndrome, Sack-Barabas type; Ehlers-Danlos Syndrome Type IV; Ehlers-Danlos syndrome vascular type
Disease Annotations     Click to see Annotation Detail View


Variant Details
Variant Transcripts
Gene Symbol:MIR3606
Accession:NR_037401
Location:EXON;NON-CODING

Gene Symbol:COL3A1
Accession:NM_000090
Location:INTRON

Variant Samples
Additional References at PubMed
PMID:28492532  


Additional Information

Database Acc Id Source(s)
ClinVar RCV003523358 CLINVAR
MedGen C0268338 CLINVAR
NCBI Gene COL3A1 CLINVAR
  MIR3606 CLINVAR
OMIM 120180 CLINVAR
  130050 CLINVAR
SNOMED CT 17025000 CLINVAR