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FLASH GENE
Symbol FAM9B contributors: mct - updated : 31-05-2023
HGNC name family with sequence similarity 9, member B
HGNC id 18404
ASSOCIATED DISORDERS
corresponding disease(s)
Susceptibility to variation of testosterone level
Variant & Polymorphism SNP
  • rs5934505 was the most significant SNP at Xp22 associated with serum T levels
  • Candidate gene
    Marker
    Therapy target
    ANIMAL & CELL MODELS