RGD:156376279 Rat Genome Database

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Variant: RGD:156376279 -  Homo sapiens

RGD ID: 156376279
ClinVar ID: CV1917652
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: COL3A1  LOC126806446  
Reference Nucleotide: T
Variant Nucleotide: G
Position
Assembly Chr Position
GRCh37 2 189,867,091
GRCh38 2 189,002,365
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.2445+14T>G
LRG_3:g.32993T>G
NG_007404.1:g.32993T>G
NG_082766.1:g.982T>G
More... 		07/21/2022 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:COL3A1
Accession:NM_000090
Location:INTRON

Variant Samples
Additional References at PubMed
PMID:28492532  


Additional Information

Database Acc Id Source(s)
ClinVar RCV002603608 CLINVAR
MedGen C0268338 CLINVAR
NCBI Gene COL3A1 CLINVAR
  LOC126806446 CLINVAR
OMIM 120180 CLINVAR
  130050 CLINVAR
SNOMED CT 17025000 CLINVAR