rs7901902

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rs7901902 has 2 RGD Records - Homo sapiens

  
Variant Page Assembly Chr Position Type Reference Nucleotide Variant Nucleotide Location Name Is Damaging? Visualize
1. View more GRCh37 10 13,330,395 - 13,330,396 snv C T EXON -
2. View more GRCh38 10 13,288,395 - 13,288,396 snv C ? - -