rs6938647

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rs6938647 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 6 160,565,883 - 160,565,884 snv A A INTRON -
2. View more GRCh38 6 160,565,883 - 160,565,884 snv A ? INTRON -