rs141344525 Rat Genome Database

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Variant: rs141344525 -  Homo sapiens

RGD ID: 15146981
RS ID: rs141344525
ClinVar ID: CV779782
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: ENO2  
Reference Nucleotide: A
Variant Nucleotide: C
Position
Assembly Chr Position
GRCh37 12 7,026,736
GRCh38 12 6,917,572
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_001975.3:c.311-9A>C
NC_000012.12:g.6917572A>C
NC_000012.11:g.7026736A>C
NM_001975.2:c.311-9A>C
 05/24/2018 intron variant benign none provided

Variant Details
Variant Transcripts
Gene Symbol:ENO2
Accession:NM_001975
Location:INTRON

Variant Samples
Additional References at PubMed
PMID:28492532  


Additional Information

Database Acc Id Source(s)
ClinVar RCV000967251 CLINVAR
dbSNP (RS) rs141344525 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene ENO2 CLINVAR
OMIM 131360 CLINVAR