rs113313325 Rat Genome Database

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Variant: rs113313325 -  Homo sapiens

RGD ID: 150415443
RS ID: rs113313325
ClinVar ID: CV1192372
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: MYH9  
Reference Nucleotide: T
Variant Nucleotide: G
Position
Assembly Chr Position
GRCh37 22 36,684,100
GRCh38 22 36,288,054
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_002473.6:c.4932+198A>C
LRG_567:g.104965A>C
NG_011884.2:g.104965A>C
NC_000022.10:g.36684100T>G
More... 		01/13/2019 intron variant likely benign none provided

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

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV001567987 CLINVAR
dbSNP (RS) rs113313325 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene MYH9 CLINVAR
OMIM 160775 CLINVAR