RGD:156087652 Rat Genome Database

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Variant: RGD:156087652 -  Homo sapiens

RGD ID: 156087652
ClinVar ID: CV2060646
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: DNASE2  LOC117125588  
Reference Nucleotide: G
Variant Nucleotide: C
Position
Assembly Chr Position
GRCh37 19 12,992,084
GRCh38 19 12,881,270
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NG_068126.1:g.100G>C
NC_000019.10:g.12881270G>C
NC_000019.9:g.12992084G>C
NM_001375.3:c.86+20C>G
 05/21/2022 intron variant likely benign none provided

Variant Details
Variant Transcripts
Gene Symbol:DNASE2
Accession:NM_001375
Location:INTRON

Variant Samples
Additional References at PubMed
PMID:28492532  


Additional Information

Database Acc Id Source(s)
ClinVar RCV002824068 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene DNASE2 CLINVAR
  LOC117125588 CLINVAR
OMIM 126350 CLINVAR