rs73517714

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rs73517714 has 3 RGD Records - Homo sapiens

  
Variant Page Assembly Chr Position Type Reference Nucleotide Variant Nucleotide Location Name Is Damaging? Visualize
1. View more GRCh38 19 16,092,494 - 16,092,495 snv C A INTRON -
2. View more GRCh38 19 16,092,494 - 16,092,495 snv C ? INTRON -
3. View more GRCh38 19 16,092,494 - 16,092,495 snv C C INTRON -