rs12136952

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rs12136952 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 1 12,601,409 - 12,601,410 snv G C INTRON;5UTRS;EXON -
2. View more GRCh38 1 12,601,409 - 12,601,410 snv G ? INTRON;5UTRS;EXON -