rs150353

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rs150353 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 15 89,384,958 - 89,384,959 snv T G INTRON;NON-CODING -
2. View more GRCh38 15 89,384,958 - 89,384,959 snv T T INTRON;NON-CODING -