RGD:150330806 Rat Genome Database

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Variant: RGD:150330806 -  Homo sapiens

RGD ID: 150330806
RS ID: rs2812357
ClinVar ID: CV1169337
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: IL11RA  
Reference Nucleotide: T
Variant Nucleotide: C
Position
Assembly Chr Position
GRCh37 9 34,655,436
GRCh38 9 34,655,439
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NC_000009.12:g.34655439T>C
NM_001142784.3:c.100+122T>C
NC_000009.11:g.34655436T>C
NG_028966.1:g.8255T>C
 10/16/2018 intron variant benign none provided

Variant Details
Variant Transcripts
Gene Symbol:IL11RA
Accession:NM_001142784
Location:INTRON

Gene Symbol:IL11RA
Accession:NR_052010
Location:INTRON;NON-CODING

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV001536139 CLINVAR
dbSNP (RS) rs2812357 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene IL11RA CLINVAR
OMIM 600939 CLINVAR