rs2046045

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rs2046045 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 5 77,239,986 - 77,239,987 snv T G INTRON;5UTRS -
2. View more GRCh38 5 77,239,986 - 77,239,987 snv T T INTRON;5UTRS -