rs375308802 Rat Genome Database

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Variant: rs375308802 -  Homo sapiens

RGD ID: 152030636
RS ID: rs375308802
ClinVar ID: CV1632243
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: CSGALNACT1  
Reference Nucleotide: G
Variant Nucleotide: A
Position
Assembly Chr Position
GRCh37 8 19,266,109
GRCh38 8 19,408,598
JBrowse: View Region in Genome Browser (JBrowse)
Model



HGVS Name(s)
Last Evaluated
Molecular Consequence
Clinical Significance
Trait Synonyms
NM_001130518.2:c.1309+15C>T
NM_001354475.2:c.1309+15C>T
NM_001354476.2:c.1309+15C>T
NM_001354483.2:c.1309+15C>T
More... 		01/26/2024 intron variant benign none provided; RECLASSIFIED - ADRA2C POLYMORPHISM; RECLASSIFIED - ADRB1 POLYMORPHISM

Gene Symbol:CSGALNACT1
Accession:NM_018371
Location:INTRON

Gene Symbol:CSGALNACT1
Accession:NM_001130518
Location:INTRON

Gene Symbol:CSGALNACT1
Accession:XM_006716363
Location:INTRON

Gene Symbol:CSGALNACT1
Accession:XM_006716360
Location:INTRON

Gene Symbol:CSGALNACT1
Accession:XM_006716364
Location:INTRON

Gene Symbol:CSGALNACT1
Accession:XM_011544578
Location:INTRON

Gene Symbol:CSGALNACT1
Accession:XM_011544583
Location:INTRON

Gene Symbol:CSGALNACT1
Accession:XM_011544585
Location:INTRON

Gene Symbol:CSGALNACT1
Accession:XM_017013625
Location:INTRON

Gene Symbol:CSGALNACT1
Accession:NM_001354476
Location:INTRON

Gene Symbol:CSGALNACT1
Accession:NM_001354481
Location:INTRON

Gene Symbol:CSGALNACT1
Accession:NM_001354477
Location:INTRON

Gene Symbol:CSGALNACT1
Accession:NM_001354480
Location:INTRON

Gene Symbol:CSGALNACT1
Accession:NM_001354475
Location:INTRON

Gene Symbol:CSGALNACT1
Accession:XM_024447193
Location:INTRON

Gene Symbol:CSGALNACT1
Accession:NM_001354483
Location:INTRON

Gene Symbol:CSGALNACT1
Accession:NM_001354487
Location:INTRON

Gene Symbol:CSGALNACT1
Accession:NM_001354489
Location:INTRON

Gene Symbol:CSGALNACT1
Accession:NM_001354485
Location:INTRON

Gene Symbol:CSGALNACT1
Accession:NM_001354484
Location:INTRON

Gene Symbol:CSGALNACT1
Accession:NM_001354488
Location:INTRON

Gene Symbol:CSGALNACT1
Accession:NM_001354490
Location:INTRON

Gene Symbol:CSGALNACT1
Accession:XM_024447192
Location:INTRON

Gene Symbol:CSGALNACT1
Accession:XM_024447191
Location:INTRON

Gene Symbol:CSGALNACT1
Accession:XM_024447190
Location:INTRON

Gene Symbol:CSGALNACT1
Accession:NM_001354497
Location:INTRON

Gene Symbol:CSGALNACT1
Accession:NM_001354492
Location:INTRON

Gene Symbol:CSGALNACT1
Accession:NM_001354495
Location:INTRON

Gene Symbol:CSGALNACT1
Accession:NM_001354494
Location:INTRON

Gene Symbol:CSGALNACT1
Accession:NM_001354496
Location:INTRON

Gene Symbol:CSGALNACT1
Accession:NM_001354499
Location:INTRON

Gene Symbol:CSGALNACT1
Accession:NM_001354491
Location:INTRON

Gene Symbol:CSGALNACT1
Accession:NM_001354498
Location:INTRON

Gene Symbol:CSGALNACT1
Accession:XM_047421960
Location:INTRON

Gene Symbol:CSGALNACT1
Accession:XM_047421971
Location:INTRON

Gene Symbol:CSGALNACT1
Accession:XM_047421964
Location:INTRON

Gene Symbol:CSGALNACT1
Accession:XM_047421977
Location:INTRON

Gene Symbol:CSGALNACT1
Accession:XM_047421961
Location:INTRON

Gene Symbol:CSGALNACT1
Accession:XM_047421969
Location:INTRON

Gene Symbol:CSGALNACT1
Accession:XM_047421976
Location:INTRON

Gene Symbol:CSGALNACT1
Accession:XM_047421965
Location:INTRON

Gene Symbol:CSGALNACT1
Accession:XM_047421972
Location:INTRON

Gene Symbol:CSGALNACT1
Accession:XM_047421973
Location:INTRON

Gene Symbol:CSGALNACT1
Accession:XM_047421975
Location:INTRON

Gene Symbol:CSGALNACT1
Accession:XM_047421963
Location:INTRON

Gene Symbol:CSGALNACT1
Accession:XM_047421962
Location:INTRON

Gene Symbol:CSGALNACT1
Accession:XM_047421968
Location:INTRON

Gene Symbol:CSGALNACT1
Accession:XM_047421979
Location:INTRON

Gene Symbol:CSGALNACT1
Accession:XM_047421970
Location:INTRON

Gene Symbol:CSGALNACT1
Accession:XM_047421974
Location:INTRON

Gene Symbol:CSGALNACT1
Accession:XM_047421978
Location:INTRON

Gene Symbol:CSGALNACT1
Accession:XM_047421967
Location:INTRON

Gene Symbol:CSGALNACT1
Accession:XM_047421966
Location:INTRON

Gene Symbol:CSGALNACT1
Accession:NR_024040
Location:INTRON;NON-CODING

Gene Symbol:CSGALNACT1
Accession:NR_148898
Location:INTRON;NON-CODING

Gene Symbol:CSGALNACT1
Accession:NR_148897
Location:INTRON;NON-CODING

Gene Symbol:CSGALNACT1
Accession:NR_148900
Location:INTRON;NON-CODING

Gene Symbol:CSGALNACT1
Accession:NR_148899
Location:INTRON;NON-CODING

Gene Symbol:CSGALNACT1
Accession:NR_148901
Location:INTRON;NON-CODING

Gene Symbol:CSGALNACT1
Accession:NR_148902
Location:INTRON;NON-CODING

Gene Symbol:CSGALNACT1
Accession:XR_007060745
Location:INTRON;NON-CODING

.
PMID:28492532  



Database
Acc Id
Source(s)
ClinVar RCV002124377 CLINVAR
dbSNP (RS) rs375308802 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene CSGALNACT1 CLINVAR
OMIM 616615 CLINVAR