rs143353512

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rs143353512 has 2 RGD Records - Homo sapiens

  
Variant Page Assembly Chr Position Type Reference Nucleotide Variant Nucleotide Location Name Is Damaging? Visualize
1. View more GRCh38 1 10,673,022 - 10,673,023 snv G A INTRON -
2. View more GRCh38 1 10,673,022 - 10,673,023 snv G ? INTRON -