rs77335224

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rs77335224 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 10 102,876,519 - 102,876,520 snv C T INTRON;NON-CODING -
2. View more GRCh38 10 102,876,519 - 102,876,520 snv C ? INTRON;NON-CODING -