rs43100 Rat Genome Database

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Variant: rs43100 -  Homo sapiens

RGD ID: 150456946
RS ID: rs43100
ClinVar ID: CV1260076
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: SRI  SRI-AS1  
Reference Nucleotide: C
Variant Nucleotide: T
Position
Assembly Chr Position
GRCh37 7 87,849,579
GRCh38 7 88,220,264
JBrowse: View Region in Genome Browser (JBrowse)
Model



HGVS Name(s)
Last Evaluated
Molecular Consequence
Clinical Significance
Trait Synonyms
NM_001256892.2:c.7-1322G>A
NM_198901.2:c.7-1322G>A
LRG_414:g.11730G>A
NG_032138.1:g.11730G>A
More... 		05/15/2021 intron variant benign none provided; RECLASSIFIED - ADRA2C POLYMORPHISM; RECLASSIFIED - ADRB1 POLYMORPHISM

Gene Symbol:SRI
Accession:NM_198901
Location:INTRON

Gene Symbol:SRI
Accession:NM_003130
Location:INTRON

Gene Symbol:SRI
Accession:NM_001256892
Location:INTRON

Gene Symbol:SRI
Accession:NM_001256891
Location:INTRON

Gene Symbol:SRI-AS1
Accession:NR_120517
Location:INTRON;NON-CODING

.
PMID:25741868  



Database
Acc Id
Source(s)
ClinVar RCV001681556 CLINVAR
dbSNP (RS) rs43100 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene SRI CLINVAR
  SRI-AS1 CLINVAR
OMIM 182520 CLINVAR