rs7586601

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rs7586601 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 2 27,361,799 - 27,361,800 snv A G INTRON;NON-CODING -
2. View more GRCh38 2 27,361,799 - 27,361,800 snv A ? INTRON;NON-CODING -