rs183574786 Rat Genome Database

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Variant: rs183574786 -  Homo sapiens

RGD ID: 15141893
RS ID: rs183574786
ClinVar ID: CV779299
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: LAMC3  
Reference Nucleotide: G
Variant Nucleotide: A
Position
Assembly Chr Position
GRCh37 9 133,932,307
GRCh38 9 131,056,920
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_006059.4:c.1940-9G>A
NG_029800.1:g.52804G>A
NC_000009.12:g.131056920G>A
NC_000009.11:g.133932307G>A
More... 		04/04/2022 intron variant benign|likely benign Cortical malformations, occipital; none provided
Disease Annotations     Click to see Annotation Detail View


Variant Details
Variant Transcripts
Gene Symbol:LAMC3
Accession:XM_011518121
Location:INTRON

Gene Symbol:LAMC3
Accession:XM_006716921
Location:INTRON

Gene Symbol:LAMC3
Accession:NM_006059
Location:INTRON

Variant Samples
Additional References at PubMed
PMID:25741868   PMID:28492532  


Additional Information

Database Acc Id Source(s)
ClinVar RCV000966381 CLINVAR
  RCV002489387 CLINVAR
dbSNP (RS) rs183574786 CLINVAR
MedGen C3279875 CLINVAR
  C3661900 CLINVAR
NCBI Gene LAMC3 CLINVAR
OMIM 604349 CLINVAR
  614115 CLINVAR