RGD:11095286 Rat Genome Database

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Variant: RGD:11095286 -  Homo sapiens

RGD ID: 11095286
RS ID: rs876657522
ClinVar ID: CV231150
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: MYH9  
Reference Nucleotide: C
Variant Nucleotide: T
Position
Assembly Chr Position
GRCh37 22 36,689,360
GRCh38 22 36,293,314
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
LRG_567:g.99705G>A
NG_011884.2:g.99705G>A
NC_000022.11:g.36293314C>T
NC_000022.10:g.36689360C>T
More... 		12/31/2015 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 RCV000222120 CLINVAR
dbSNP (RS) rs876657522 CLINVAR
MedGen CN169374 CLINVAR
NCBI Gene MYH9 CLINVAR
OMIM 160775 CLINVAR