rs438811

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rs438811 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 19 44,913,484 - 44,913,485 snv C T - -
2. View more GRCh38 19 44,913,484 - 44,913,485 snv C C - -
3. View more GRCh38 19 44,913,484 - 44,913,485 snv C ? - -