rs35742417

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rs35742417 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 6 7,247,111 - 7,247,112 snv C A EXON;INTRON -
2. View more GRCh38 6 7,247,111 - 7,247,112 snv C C EXON;INTRON -
3. View more GRCh38 6 7,247,111 - 7,247,112 snv C ? EXON;INTRON -