rs7182178

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rs7182178 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 15 49,843,371 - 49,843,372 snv T C - -
2. View more GRCh38 15 49,832,202 - 49,832,203 snv T T - -