RGD:11622674 Rat Genome Database

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Variant: RGD:11622674 -  Homo sapiens

RGD ID: 11622674
RS ID: rs59312184
ClinVar ID: CV331377
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: SLCO1B3  
Reference Nucleotide: G
Variant Nucleotide: A
Position
Assembly Chr Position
GRCh37 12 20,963,638
GRCh38 12 20,810,704
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Age of Onset Prevalence Trait Synonyms
NC_000012.12:g.20810704G>A
NC_000012.11:g.20963638G>A
NM_019844.3:c.-241G>A
NG_032071.1:g.5001G>A
More... 		01/13/2018 5 prime utr variant benign|likely benign all ages <1 / 1 000 000 Hyperbilirubinemia, Rotor type; HYPERBILIRUBINEMIA, ROTOR TYPE, DIGENIC
Disease Annotations     Click to see Annotation Detail View


Variant Details
Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV000363014 CLINVAR
dbSNP (RS) rs59312184 CLINVAR
MedGen C0220991 CLINVAR
NCBI Gene SLCO1B3 CLINVAR
OMIM 237450 CLINVAR
  605495 CLINVAR
SNOMED CT 32891000 CLINVAR