rs4409766

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rs4409766 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 10 102,856,906 - 102,856,907 snv T C INTRON;NON-CODING -
2. View more GRCh38 10 102,856,906 - 102,856,907 snv T ? INTRON;NON-CODING -
3. View more GRCh38 10 102,856,906 - 102,856,907 snv T T INTRON;NON-CODING -