rs72852050 Rat Genome Database

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Variant: rs72852050 -  Homo sapiens

RGD ID: 15113687
RS ID: rs72852050
ClinVar ID: CV779038
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: ADAMTS3  
Reference Nucleotide: C
Variant Nucleotide: T
Position
Assembly Chr Position
GRCh37 4 73,280,525
GRCh38 4 72,414,808
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_014243.3:c.661+7G>A
NG_046955.1:g.158992G>A
NC_000004.12:g.72414808C>T
NC_000004.11:g.73280525C>T
More... 		11/29/2021 intron variant benign|likely benign ADAMTS3-related condition; none provided
Disease Annotations     Click to see Annotation Detail View


Variant Details
Variant Transcripts
Gene Symbol:ADAMTS3
Accession:XM_011532422
Location:INTRON

Gene Symbol:ADAMTS3
Accession:XM_011532421
Location:INTRON

Gene Symbol:ADAMTS3
Accession:NM_014243
Location:INTRON

Variant Samples
Additional References at PubMed
PMID:25741868   PMID:28492532  


Additional Information

Database Acc Id Source(s)
ClinVar RCV000961536 CLINVAR
  RCV002505447 CLINVAR
  RCV003960713 CLINVAR
dbSNP (RS) rs72852050 CLINVAR
MedGen C3661900 CLINVAR
  C4748408 CLINVAR
NCBI Gene ADAMTS3 CLINVAR
OMIM 605011 CLINVAR
  618154 CLINVAR