rs7732130

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rs7732130 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 5 77,139,179 - 77,139,180 snv G A INTRON;NON-CODING;5UTRS -
2. View more GRCh38 5 77,139,179 - 77,139,180 snv G G INTRON;NON-CODING;5UTRS -