RGD:407484741 Rat Genome Database

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Variant: RGD:407484741 -  Homo sapiens

RGD ID: 407484741
ClinVar ID: CV3449682
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: MAGI2  MAGI2-AS3  
Reference Nucleotide: A
Variant Nucleotide: G
Position
Assembly Chr Position
GRCh37 7 79,082,612
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_001301128.2:c.25A>G
NM_012301.4:c.25A>G
NG_011487.2:g.5279A>G
NC_000007.14:g.79453296T>C
More... 		04/15/2024 missense variant uncertain significance AllHighlyPenetrant

Variant Details
Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV004640581 CLINVAR
MedGen CN169374 CLINVAR
NCBI Gene MAGI2 CLINVAR
  MAGI2-AS3 CLINVAR
OMIM 606382 CLINVAR