rs760740919 Rat Genome Database

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Variant: rs760740919 -  Homo sapiens

RGD ID: 152032604
RS ID: rs760740919
ClinVar ID: CV1614828
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: WRAP53  
Reference Nucleotide: T
Variant Nucleotide: C
Position
Assembly Chr Position
GRCh37 17 7,604,765
GRCh38 17 7,701,447
JBrowse: View Region in Genome Browser (JBrowse)
Model



HGVS Name(s)
Last Evaluated
Molecular Consequence
Clinical Significance
Trait Synonyms
LRG_375t1:c.732-12T>C
NM_001143990.2:c.732-12T>C
NM_018081.2:c.732-12T>C
NM_001143991.2:c.732-12T>C
More... 		04/24/2021 intron variant likely benign none provided; RECLASSIFIED - ADRA2C POLYMORPHISM; RECLASSIFIED - ADRB1 POLYMORPHISM

Gene Symbol:WRAP53
Accession:NM_001143990
Location:INTRON

Gene Symbol:WRAP53
Accession:NM_001143991
Location:INTRON

Gene Symbol:WRAP53
Accession:NM_018081
Location:INTRON

Gene Symbol:WRAP53
Accession:NM_001143992
Location:INTRON

.
PMID:28492532  



Database
Acc Id
Source(s)
ClinVar RCV002086611 CLINVAR
dbSNP (RS) rs760740919 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene WRAP53 CLINVAR
OMIM 612661 CLINVAR