rs11836976 Rat Genome Database

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Variant: rs11836976 -  Homo sapiens

RGD ID: 150504247
RS ID: rs11836976
ClinVar ID: CV1285919
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: PRPH  TROAP-AS1  
Reference Nucleotide: T
Variant Nucleotide: C
Position
Assembly Chr Position
GRCh37 12 49,691,707
GRCh38 12 49,297,924
JBrowse: View Region in Genome Browser (JBrowse)
Model



HGVS Name(s)
Last Evaluated
Molecular Consequence
Clinical Significance
Trait Synonyms
NM_006262.4:c.1268-34T>C
NG_008354.1:g.7799T>C
NC_000012.12:g.49297924T>C
NC_000012.11:g.49691707T>C
 05/20/2019 intron variant benign none provided

Gene Symbol:PRPH
Accession:NM_006262
Location:INTRON

Gene Symbol:TROAP-AS1
Accession:NR_120449
Location:INTRON;NON-CODING

.
PMID:25741868  



Database
Acc Id
Source(s)
ClinVar RCV001719342 CLINVAR
dbSNP (RS) rs11836976 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene PRPH CLINVAR
  TROAP-AS1 CLINVAR
OMIM 170710 CLINVAR