rs11249215

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rs11249215 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 1 24,970,693 - 24,970,694 snv G A - -
2. View more GRCh38 1 24,970,693 - 24,970,694 snv G ? - -