rs10251347

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rs10251347 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 7 148,117,446 - 148,117,447 snv C G 3UTRS;EXON -
2. View more GRCh38 7 148,420,354 - 148,420,355 snv C ? - -