rs12913832

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rs12913832 has 3 RGD Records - Homo sapiens

  
Variant Page Assembly Chr Position Type Reference Nucleotide Variant Nucleotide Location Name Is Damaging? Visualize
1. View more GRCh37 15 28,365,618 - 28,365,619 snv A G INTRON -
2. View more GRCh38 15 28,120,472 - 28,120,473 snv A A - -
3. View more GRCh38 15 28,120,472 - 28,120,473 snv A ? - -