rs56282503

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rs56282503 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 40,274,558 - 40,274,559 snv T ? INTRON -
2. View more GRCh38 15 40,274,558 - 40,274,559 snv T T INTRON -