RS201054877 FGFR1

Health Risk Chr 8:38428379
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Associated Conditions
Hypogonadotropic hypogonadism 2 with or without anosmia
Osteoglophonic dysplasia
Craniosynostosis syndrome
Trigonocephaly 1
Pfeiffer syndrome
Inborn genetic diseases
Hypogonadotropic hypogonadism 2 with or without anosmia
Osteoglophonic dysplasia
Craniosynostosis syndrome
Trigonocephaly 1
Pfeiffer syndrome
Inborn genetic diseases
Other Variants in FGFR1
rs121909627 rs1586111679 rs1563433902 rs121909628 rs121909629 rs1586287678 rs121909630 rs121909632 rs121909631 rs121909633
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