rs62155873

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rs62155873 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 2 105,352,905 - 105,352,906 snv C T 3UTRS;INTRON;NON-CODING -
2. View more GRCh38 2 105,352,905 - 105,352,906 snv C ? INTRON;NON-CODING;3UTRS -
3. View more GRCh38 2 105,352,905 - 105,352,906 snv C C INTRON;3UTRS;NON-CODING -