RGD:9690834 Rat Genome Database

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Variant: RGD:9690834 -  Homo sapiens

RGD ID: 9690834
RS ID: rs727505086
ClinVar ID: CV176252
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: MYH9  
Reference Nucleotide: C
Variant Nucleotide: G
Position
Assembly Chr Position
GRCh37 22 36,680,570
GRCh38 22 36,284,524
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.36284524C>G
NC_000022.10:g.36680570C>G
NM_002473.4:c.5484-13G>C
LRG_567:g.108495G>C
More... 		05/23/2014 intron variant likely benign AllHighlyPenetrant

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

Variant Samples
Additional References at PubMed
PMID:24033266  


Additional Information

Database Acc Id Source(s)
ClinVar RCV000156526 CLINVAR
dbSNP (RS) rs727505086 CLINVAR
MedGen CN169374 CLINVAR
NCBI Gene MYH9 CLINVAR
OMIM 160775 CLINVAR