rs4457054

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rs4457054 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 77,129,235 - 77,129,236 snv G C INTRON;NON-CODING;5UTRS -
2. View more GRCh38 5 77,129,235 - 77,129,236 snv G G - -