rs11922042

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rs11922042 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 3 12,164,989 - 12,164,990 snv T C INTRON -
2. View more GRCh38 3 12,164,989 - 12,164,990 snv T T INTRON -