RGD:28897696 Rat Genome Database

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Variant: RGD:28897696 -  Homo sapiens

RGD ID: 28897696
RS ID: rs183992670
ClinVar ID: CV867727
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: CSRP3-AS1  
Reference Nucleotide: G
Variant Nucleotide: A
Position
Assembly Chr Position
GRCh37 11 19,232,090
GRCh38 11 19,210,543
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Clinical Significance Trait Synonyms
NC_000011.10:g.19210543G>A
NC_000011.9:g.19232090G>A
LRG_440:g.5031C>T
NG_011932.2:g.5031C>T
More... 		01/12/2018 uncertain significance Familial hypertrophic cardiomyopathy 12
Disease Annotations     Click to see Annotation Detail View


Variant Details
Variant Transcripts
Gene Symbol:
Accession:
Location:INTRON;NON-CODING

Gene Symbol:CSRP3-AS1
Accession:NR_183673
Location:INTRON;NON-CODING

Gene Symbol:CSRP3-AS1
Accession:NR_183675
Location:INTRON;NON-CODING

Gene Symbol:
Accession:
Location:INTRON;NON-CODING

Gene Symbol:
Accession:
Location:INTRON;NON-CODING

Gene Symbol:CSRP3-AS1
Accession:NR_183672
Location:INTRON;NON-CODING

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV001102703 CLINVAR
dbSNP (RS) rs183992670 CLINVAR
MedGen C2677491 CLINVAR
NCBI Gene CSRP3 CLINVAR
  CSRP3-AS1 CLINVAR
OMIM 600824 CLINVAR
  612124 CLINVAR