rs7182018

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rs7182018 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 15 39,340,068 - 39,340,069 snv A G INTRON;NON-CODING -
2. View more GRCh38 15 39,340,068 - 39,340,069 snv A ? INTRON;NON-CODING -
3. View more GRCh38 15 39,340,068 - 39,340,069 snv A A INTRON;NON-CODING -