RGD:152147327 Rat Genome Database

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Variant: RGD:152147327 -  Homo sapiens

RGD ID: 152147327
RS ID: rs777712102
ClinVar ID: CV1649728
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: LMNB2  MIR7108  
Reference Nucleotide: C
Variant Nucleotide: T
Position
Assembly Chr Position
GRCh37 19 2,434,928
GRCh38 19 2,434,930
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NC_000019.10:g.2434930G>A
NC_000019.9:g.2434928G>A
NR_106958.1:n.71C>T
NG_008355.1:g.27031C>T
More... 		12/16/2020 intron variant likely benign APLD, SUSCEPTIBILITY TO; Lipodystrophy, partial, acquired, susceptibility to
Disease Annotations     Click to see Annotation Detail View


Variant Details
Variant Transcripts
Gene Symbol:MIR7108
Accession:NR_106958
Location:EXON;NON-CODING

Gene Symbol:LMNB2
Accession:NM_032737
Location:INTRON

Variant Samples
Additional References at PubMed
PMID:28492532  


Additional Information

Database Acc Id Source(s)
ClinVar RCV002121251 CLINVAR
dbSNP (RS) rs777712102 CLINVAR
MedGen C4225289 CLINVAR
NCBI Gene LMNB2 CLINVAR
  MIR7108 CLINVAR
OMIM 150341 CLINVAR
  608709 CLINVAR
  616540 CLINVAR