Basic Information

SNP ID hsa762
Organism Homo Sapiens
Genome Assembly GRCh37
Version 1
Variation Class SNP
Position 1:799463
RefSNP Alleles T/C
Synonyms ID rs4245756

Gene Annotation

Gene ID Transcript ID Gene Symbol Variant Effect Biotype cDNA Position Allele Change Protein ID Protein Position Residue Change
ENSG00000228794 ENST00000445118 LINC01128 downstream_gene_variant lincRNA 0 - => - - 0 - => -
ENSG00000230368 ENST00000427857 FAM41C downstream_gene_variant lincRNA 0 - => - - 0 - => -
ENSG00000230368 ENST00000432963 FAM41C downstream_gene_variant lincRNA 0 - => - - 0 - => -
ENSG00000230368 ENST00000446136 FAM41C downstream_gene_variant lincRNA 0 - => - - 0 - => -

Population Diversity

Population Sample # Allele:Frequency Genotype:Frequency
EAS 215 T:0.00; C:1.00; CC:1.00;