RGD:9691984 Rat Genome Database

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Variant: RGD:9691984 -  Homo sapiens

RGD ID: 9691984
RS ID: rs727503295
ClinVar ID: CV176285
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: MYH9  
Reference Nucleotide: G
Variant Nucleotide: A
Position
Assembly Chr Position
GRCh37 22 36,744,936
GRCh38 22 36,348,891
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NC_000022.11:g.36348891G>A
NC_000022.10:g.36744936G>A
NM_002473.4:c.333+13C>T
LRG_567:g.44128C>T
More...
03/31/2015 intron variant likely benign AllHighlyPenetrant; none provided

Variant Details
Variant Transcripts
Gene Symbol:MYH9
Accession:NM_002473
Location:INTRON

Variant Samples
Additional References at PubMed
PMID:24033266   PMID:28492532  


Additional Information

Database Acc Id Source(s)
ClinVar RCV000151359 CLINVAR
  RCV003764914 CLINVAR
dbSNP (RS) rs727503295 CLINVAR
MedGen C3661900 CLINVAR
  CN169374 CLINVAR
NCBI Gene MYH9 CLINVAR
OMIM 160775 CLINVAR