rs2150121906 Rat Genome Database

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Variant: rs2150121906 -  Homo sapiens

RGD ID: 153303566
RS ID: rs2150121906
ClinVar ID: CV1686357
Genic Status: GENIC
Type: deletion (SO:0000159) 
Associated Genes: SCP2  
Reference Nucleotide: TA
Variant Nucleotide: -
Position
Assembly Chr Position
GRCh37 1 53,413,744 - 53,413,746
GRCh38 1 52,948,072 - 52,948,074
JBrowse: View Region in Genome Browser (JBrowse)
Model



HGVS Name(s)
Last Evaluated
Molecular Consequence
Clinical Significance
Trait Synonyms
NM_001007098.3:c.191_192del
NM_001193600.2:c.191_192del
NM_001330587.2:c.191_192del
NM_002979.5:c.191_192del
More... 		05/11/2023 5 prime utr variant conflicting interpretations of pathogenicity|uncertain significance none provided; RECLASSIFIED - ADRA2C POLYMORPHISM; RECLASSIFIED - ADRB1 POLYMORPHISM

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PMID:16685654   PMID:25741868   PMID:26497993   PMID:28492532  



Database
Acc Id
Source(s)
ClinVar RCV002261790 CLINVAR
dbSNP (RS) rs2150121906 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene SCP2 CLINVAR
OMIM 184755 CLINVAR