Basic Information

SNP ID hsa19
Organism Homo Sapiens
Genome Assembly GRCh37
Version 1
Variation Class SNP
Position 1:55299
RefSNP Alleles C/T
Synonyms ID rs10399749

Gene Annotation

Gene ID Transcript ID Gene Symbol Variant Effect Biotype cDNA Position Allele Change Protein ID Protein Position Residue Change
ENSG00000268020 ENST00000594647 OR4G4P downstream_gene_variant unprocessed_pseudogene 0 - => - - 0 - => -
ENSG00000268020 ENST00000606857 OR4G4P downstream_gene_variant unprocessed_pseudogene 0 - => - - 0 - => -

Population Diversity

Population Sample # Allele:Frequency Genotype:Frequency
EAS 215 C:0.68; T:0.32; CC:0.42; CT:0.53; TT:0.05;