rs1888909

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Pathways
rs1888909 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 9 6,197,392 - 6,197,393 snv T C - -
2. View more GRCh38 9 6,197,392 - 6,197,393 snv T T - -