rs9912468

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rs9912468 has 3 RGD Records - Homo sapiens

  
Variant Page Assembly Chr Position Type Reference Nucleotide Variant Nucleotide Location Name Is Damaging? Visualize
1. View more GRCh38 17 66,322,239 - 66,322,240 snv G C INTRON;NON-CODING;5UTRS -
2. View more GRCh38 17 66,322,239 - 66,322,240 snv G G INTRON;NON-CODING;5UTRS -
3. View more GRCh38 17 66,322,239 - 66,322,240 snv G ? INTRON;5UTRS;NON-CODING -