rs1695928041 Rat Genome Database

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Variant: rs1695928041 -  Homo sapiens

RGD ID: 152149176
RS ID: rs1695928041
ClinVar ID: CV1552212
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: DIS3L2  
Reference Nucleotide: G
Variant Nucleotide: T
Position
Assembly Chr Position
GRCh37 2 233,200,601
GRCh38 2 232,335,891
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_001257281.2:c.1582-7454G>T
NM_152383.5:c.2496+17G>T
LRG_534:g.379309G>T
NG_032572.1:g.379309G>T
More... 		10/19/2021 intron variant likely benign Nephroblastomatosis fetal ascites macrosomia and wilms tumor; Renal hamartomas nephroblastomatosis and fetal gigantism
Disease Annotations     Click to see Annotation Detail View


Variant Details
Variant Transcripts
Gene Symbol:DIS3L2
Accession:NR_046477
Location:EXON;NON-CODING

Gene Symbol:DIS3L2
Accession:NM_001257282
Location:INTRON

Gene Symbol:DIS3L2
Accession:NM_152383
Location:INTRON

Gene Symbol:DIS3L2
Accession:NM_001257281
Location:INTRON

Gene Symbol:DIS3L2
Accession:NR_046476
Location:INTRON;NON-CODING

Variant Samples
Additional References at PubMed
PMID:28492532  


Additional Information

Database Acc Id Source(s)
ClinVar RCV002157907 CLINVAR
dbSNP (RS) rs1695928041 CLINVAR
MedGen C0796113 CLINVAR
NCBI Gene DIS3L2 CLINVAR
OMIM 267000 CLINVAR
  614184 CLINVAR