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variants: 5427938

One row per variant. Variant_ID = Chromosome:Position:Ref:Alt (GRCh38). Allele frequencies are gnomAD v4.1 joint (joint + 8 ancestries). Free-text search box covers rsID, gene symbol and amino-acid change.

Data license: Apache License 2.0

This data as json

rowid Variant_ID RSID Chromosome Position Reference_Allele Alternate_Allele Joint_AF African_AF Admixed_American_AF Ashkenazi_Jewish_AF East_Asian_AF Finnish_AF Middle_Eastern_AF Non_Finnish_European_AF South_Asian_AF ENCODE_cCRE_Annotation Repeat_Name Repeat_Class Repeat_Family Functional_Annotation Gene Gene_Detail Exonic_Function Amino_Acid_Change PhastCons_100way PhyloP_100way Evo2_7B_NoRC_Ref Evo2_7B_NoRC_Alt Evo2_7B_NoRC_Delta Evo2_7B_AvgRC_Ref Evo2_7B_AvgRC_Alt Evo2_7B_AvgRC_Delta Evo2_7B_WeightedRC_Ref Evo2_7B_WeightedRC_Alt Evo2_7B_WeightedRC_Delta Evo2_40B_NoRC_Ref Evo2_40B_NoRC_Alt Evo2_40B_NoRC_Delta Evo2_40B_AvgRC_Ref Evo2_40B_AvgRC_Alt Evo2_40B_AvgRC_Delta Evo2_40B_WeightedRC_Ref Evo2_40B_WeightedRC_Alt Evo2_40B_WeightedRC_Delta MAF_tier AF_bin SCREEN_V4_Classes SCREEN_V4_Accessions SCREEN_V4_Overlap_Count
5427938 6:88434149:A:G rs201337704 6 88434149 A G 0.235205 0.206687 0.177852 0.211337 0.233437 0.261237 0.287671 0.261825 0.219466 Intronic L1PA3 LINE L1 ncRNA_intronic ENSG00000234426       0.2455 0.058 -32342.142578125 -32359.44921875 -17.306640625 -32170.9873046875 -32204.58203125 -33.5947265625 -34396.9481283611 -34420.9618774231 -24.0137490620546 -20599.666015625 -16518.841796875 4080.82421875 -18164.2685546875 -16022.7841796875 2141.484375 -20201.6451409298 -17031.1709008802 3170.47424004969 Q3_40-60% AF_0.2-0.4     0
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