rs602662

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rs602662 has 3 RGD Records - Homo sapiens

  
Variant Page Assembly Chr Position Type Reference Nucleotide Variant Nucleotide Location Name Is Damaging? Visualize
1. View more GRCh37 19 49,206,985 - 49,206,986 snv G A EXON -
2. View more GRCh38 19 48,703,728 - 48,703,729 snv G G - -
3. View more GRCh38 19 48,703,728 - 48,703,729 snv G ? - -