RS201773631 FGFR1

Health Risk Chr 8:38417996
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Associated Conditions
Trigonocephaly 1
Hypogonadotropic hypogonadism 2 with or without anosmia
Osteoglophonic dysplasia
Craniosynostosis syndrome
Pfeiffer syndrome
Inborn genetic diseases
Trigonocephaly 1
Hypogonadotropic hypogonadism 2 with or without anosmia
Osteoglophonic dysplasia
Craniosynostosis syndrome
Pfeiffer syndrome
Inborn genetic diseases
Other Variants in FGFR1
rs121909627 rs1586111679 rs1563433902 rs121909628 rs121909629 rs1586287678 rs121909630 rs121909632 rs121909631 rs121909633
Ask Dr. Hemsworth about this variant