rs1060431

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rs1060431 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 17 4,937,573 - 4,937,574 snv G A 3UTRS;EXON -
2. View more GRCh38 17 4,937,573 - 4,937,574 snv G G 3UTRS;EXON -