rs198389

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rs198389 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 1 11,859,214 - 11,859,215 snv A G - -
2. View more GRCh38 1 11,859,214 - 11,859,215 snv A A - -
3. View more GRCh38 1 11,859,214 - 11,859,215 snv A ? - -