RS876661334 FGFR1

Health Risk Chr 8:38414778
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What This Variant Does
"CLNSIG=4
Associated Conditions
Semilobar holoprosencephaly
Hypogonadotropic hypogonadism 2 with or without anosmia
Pfeiffer syndrome
FGFR1-related disorder
7 conditions
Hypogonadotropic hypogonadism 2 with or without anosmia
Pfeiffer syndrome
Semilobar holoprosencephaly
Hypogonadotropic hypogonadism 2 with or without anosmia
Pfeiffer syndrome
FGFR1-related disorder
7 conditions
Hypogonadotropic hypogonadism 2 with or without anosmia
Pfeiffer syndrome
Other Variants in FGFR1
rs121909627 rs1586111679 rs1563433902 rs121909628 rs121909629 rs1586287678 rs121909630 rs121909632 rs121909631 rs121909633
Ask Dr. Hemsworth about this variant