rs78689694

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rs78689694 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 11 126,364,925 - 126,364,926 snv G C INTRON;5UTRS;NON-CODING -
2. View more GRCh38 11 126,364,925 - 126,364,926 snv G G 5UTRS;INTRON;NON-CODING -
3. View more GRCh38 11 126,364,925 - 126,364,926 snv G ? INTRON;5UTRS;NON-CODING -