rs761818772 Rat Genome Database

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Variant: rs761818772 -  Homo sapiens

RGD ID: 152031505
RS ID: rs761818772
ClinVar ID: CV1548739
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: WRAP53  
Reference Nucleotide: A
Variant Nucleotide: G
Position
Assembly Chr Position
GRCh37 17 7,604,880
GRCh38 17 7,701,562
JBrowse: View Region in Genome Browser (JBrowse)
Model



HGVS Name(s)
Last Evaluated
Molecular Consequence
Clinical Significance
Trait Synonyms
LRG_375t1:c.822+13A>G
NM_001143990.2:c.822+13A>G
NM_001143991.2:c.822+13A>G
NM_001143992.2:c.822+13A>G
More... 		06/27/2022 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 RCV002086381 CLINVAR
dbSNP (RS) rs761818772 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene WRAP53 CLINVAR
OMIM 612661 CLINVAR