RGD:8649100 Rat Genome Database

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Variant: RGD:8649100 -  Homo sapiens

RGD ID: 8649100
RS ID: rs121913205
ClinVar ID: CV116925
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: IFNGR2  
Reference Nucleotide: A
Variant Nucleotide: G
Position
Assembly Chr Position
GRCh37 21 34,799,132
GRCh38 21 33,426,825
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_005534.4:c.413-59A>G
NM_001329128.2:c.470-59A>G
NC_000021.9:g.33426825A>G
LRG_67t1:c.413-59A>G
More... 		intron|intron variant not provided none provided

Variant Details
Variant Transcripts
Gene Symbol:IFNGR2
Accession:NM_005534
Location:INTRON

Gene Symbol:IFNGR2
Accession:NM_001329128
Location:INTRON

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV000097445 CLINVAR
dbSNP (RS) rs121913205 CLINVAR
MedGen CN517202 CLINVAR
NCBI Gene IFNGR2 CLINVAR
OMIM 147569 CLINVAR