rs78879925 Rat Genome Database

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Variant: rs78879925 -  Homo sapiens

RGD ID: 150535868
RS ID: rs78879925
ClinVar ID: CV1307152
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: MAGI2  
Reference Nucleotide: A
Variant Nucleotide: G
Position
Assembly Chr Position
GRCh37 7 77,973,301
GRCh38 7 78,343,984
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.1226-24T>C
NM_012301.4:c.1226-24T>C
NG_011487.2:g.1114591T>C
NC_000007.14:g.78343984A>G
More... 		06/25/2020 intron variant likely benign none provided

Variant Details
Variant Transcripts
Gene Symbol:MAGI2
Accession:XM_017012842
Location:INTRON

Gene Symbol:MAGI2
Accession:XM_017012843
Location:INTRON

Gene Symbol:MAGI2
Accession:XM_047421093
Location:INTRON

Gene Symbol:MAGI2
Accession:NM_001301128
Location:INTRON

Gene Symbol:MAGI2
Accession:XM_017012841
Location:INTRON

Gene Symbol:MAGI2
Accession:XM_017012847
Location:INTRON

Gene Symbol:MAGI2
Accession:XM_047421092
Location:INTRON

Gene Symbol:MAGI2
Accession:XM_011516728
Location:INTRON

Gene Symbol:MAGI2
Accession:XM_017012840
Location:INTRON

Gene Symbol:MAGI2
Accession:XM_017012844
Location:INTRON

Gene Symbol:MAGI2
Accession:XM_011516718
Location:INTRON

Gene Symbol:MAGI2
Accession:XM_017012845
Location:INTRON

Gene Symbol:MAGI2
Accession:XM_017012846
Location:INTRON

Gene Symbol:MAGI2
Accession:NM_012301
Location:INTRON

Gene Symbol:MAGI2
Accession:XM_011516720
Location:INTRON

Variant Samples
Additional References at PubMed
PMID:25741868  


Additional Information

Database Acc Id Source(s)
ClinVar RCV001759207 CLINVAR
dbSNP (RS) rs78879925 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene MAGI2 CLINVAR
OMIM 606382 CLINVAR