rs1256335

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rs1256335 has 3 RGD Records - Homo sapiens

  
Variant Page
Assembly
Chr
Position
Type
Reference Nucleotide
Variant Nucleotide
Location Name
Is Damaging?
Visualize
1. View more GRCh37 1 21,890,386 - 21,890,387 snv G A INTRON -
2. View more GRCh38 1 21,563,893 - 21,563,894 snv G A - -
3. View more GRCh38 1 21,563,893 - 21,563,894 snv G ? - -