rs11216435

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rs11216435 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 11 117,518,217 - 117,518,218 snv C T INTRON -
2. View more GRCh38 11 117,518,217 - 117,518,218 snv C ? INTRON -