rs151291132

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rs151291132 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 15 44,550,012 - 44,550,013 snv A G INTRON -
2. View more GRCh38 15 44,550,012 - 44,550,013 snv A A INTRON -