rs142552223

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rs142552223 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 3 172,516,227 - 172,516,228 snv G A INTRON;NON-CODING -
2. View more GRCh38 3 172,516,227 - 172,516,228 snv G G INTRON;NON-CODING -
3. View more GRCh38 3 172,516,227 - 172,516,228 snv G ? INTRON;NON-CODING -