rs761423

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rs761423 has 3 RGD Records - Homo sapiens

  
Variant Page
Assembly
Chr
Position
Type
Reference Nucleotide
Variant Nucleotide
Location Name
Is Damaging?
Visualize
1. View more GRCh38 1 16,975,177 - 16,975,178 snv T C INTRON -
2. View more GRCh38 1 16,975,177 - 16,975,178 snv T T INTRON -
3. View more GRCh38 1 16,975,177 - 16,975,178 snv T ? INTRON -