rs11523307 Rat Genome Database

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Variant: rs11523307 -  Homo sapiens

RGD ID: 150336882
RS ID: rs11523307
ClinVar ID: CV1171936
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: MYMK  
Reference Nucleotide: A
Variant Nucleotide: G
Position
Assembly Chr Position
GRCh37 9 136,384,162
GRCh38 9 133,519,040
JBrowse: View Region in Genome Browser (JBrowse)
Model



HGVS Name(s)
Last Evaluated
Molecular Consequence
Clinical Significance
Trait Synonyms
NM_001080483.3:c.251-18T>C
NC_000009.12:g.133519040A>G
NC_000009.11:g.136384162A>G
 05/17/2021 intron variant benign none provided

Gene Symbol:MYMK
Accession:NM_001080483
Location:INTRON

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PMID:25741868  



Database
Acc Id
Source(s)
ClinVar RCV001541252 CLINVAR
dbSNP (RS) rs11523307 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene MYMK CLINVAR
OMIM 615345 CLINVAR