rs2070761 Rat Genome Database

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Variant: rs2070761 -  Homo sapiens

RGD ID: 150440866
RS ID: rs2070761
ClinVar ID: CV1220228
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: PRPH  TROAP-AS1  
Reference Nucleotide: T
Variant Nucleotide: C
Position
Assembly Chr Position
GRCh37 12 49,690,509
GRCh38 12 49,296,726
JBrowse: View Region in Genome Browser (JBrowse)
Model



HGVS Name(s)
Last Evaluated
Molecular Consequence
Clinical Significance
Trait Synonyms
NM_006262.4:c.703-163T>C
NG_008354.1:g.6601T>C
NC_000012.12:g.49296726T>C
NC_000012.11:g.49690509T>C
More... 		08/31/2018 intron variant benign none provided

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

Gene Symbol:PRPH
Accession:NM_006262
Location:INTRON

.
PMID:25741868  



Database
Acc Id
Source(s)
ClinVar RCV001610211 CLINVAR
dbSNP (RS) rs2070761 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene PRPH CLINVAR
  TROAP-AS1 CLINVAR
OMIM 170710 CLINVAR