rs41271151

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Pathways
rs41271151 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 9 23,692,127 - 23,692,128 snv C G 3UTRS;EXON;INTRON -
2. View more GRCh38 9 23,692,127 - 23,692,128 snv C C 3UTRS;EXON;INTRON -