rs754993 Rat Genome Database

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Variant: rs754993 -  Homo sapiens

RGD ID: 150477069
RS ID: rs754993
ClinVar ID: CV1239977
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: DNAJC13  
Reference Nucleotide: G
Variant Nucleotide: A
Position
Assembly Chr Position
GRCh37 3 132,244,406
GRCh38 3 132,525,562
JBrowse: View Region in Genome Browser (JBrowse)
Model



HGVS Name(s)
Last Evaluated
Molecular Consequence
Clinical Significance
Trait Synonyms
NM_015268.4:c.6061-48G>A
NM_001329126.2:c.6076-48G>A
NG_051045.1:g.113036G>A
NC_000003.12:g.132525562G>A
More... 		07/09/2018 intron variant benign none provided

Gene Symbol:DNAJC13
Accession:NM_015268
Location:INTRON

Gene Symbol:DNAJC13
Accession:NM_001329126
Location:INTRON

Gene Symbol:DNAJC13
Accession:XM_047447819
Location:INTRON

Gene Symbol:DNAJC13
Accession:XM_047447820
Location:INTRON

.
PMID:25741868  



Database
Acc Id
Source(s)
ClinVar RCV001652155 CLINVAR
dbSNP (RS) rs754993 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene DNAJC13 CLINVAR
OMIM 614334 CLINVAR