rs814518

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rs814518 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 19 40,578,787 - 40,578,788 snv G A INTRON;5UTRS -
2. View more GRCh38 19 40,578,787 - 40,578,788 snv G ? INTRON;5UTRS -