rs11636073

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rs11636073 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 15 48,246,829 - 48,246,830 snv A T INTRON -
2. View more GRCh37 15 48,539,026 - 48,539,027 snv A G INTRON -