RGD:152032456 Rat Genome Database

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Variant: RGD:152032456 -  Homo sapiens

RGD ID: 152032456
RS ID: rs1476532102
ClinVar ID: CV1629417
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: IL36RN  
Reference Nucleotide: C
Variant Nucleotide: A
Position
Assembly Chr Position
GRCh37 2 113,817,059
GRCh38 2 113,059,482
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NG_031864.1:g.5845C>A
NC_000002.12:g.113059482C>A
NC_000002.11:g.113817059C>A
LRG_730t1:c.29+15C>A
More... 		07/01/2021 intron variant likely benign
Disease Annotations     Click to see Annotation Detail View


Variant Details
Variant Transcripts
Gene Symbol:IL36RN
Accession:NM_012275
Location:INTRON

Gene Symbol:IL36RN
Accession:NM_173170
Location:INTRON

Gene Symbol:IL36RN
Accession:XM_047443918
Location:INTRON

Variant Samples
Additional References at PubMed
PMID:28492532  


Additional Information

Database Acc Id Source(s)
ClinVar RCV002106369 CLINVAR
dbSNP (RS) rs1476532102 CLINVAR
MedGen C0343055 CLINVAR
NCBI Gene IL36RN CLINVAR
OMIM 605507 CLINVAR
  614204 CLINVAR
SNOMED CT 238612002 CLINVAR