rs1294421

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rs1294421 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 6 6,742,916 - 6,742,917 snv T G INTRON;NON-CODING -
2. View more GRCh38 6 6,742,916 - 6,742,917 snv T T INTRON;NON-CODING -
3. View more GRCh38 6 6,742,916 - 6,742,917 snv T ? INTRON;NON-CODING -