rs1618332

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rs1618332 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 41,892,596 - 41,892,597 snv T C INTRON;NON-CODING -
2. View more GRCh38 15 41,892,596 - 41,892,597 snv T ? INTRON;NON-CODING -