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Items: 4

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
FGFR1
(R529Q +7 more)
Single nucleotide variant
(missense variant)
Hartsfield-Bixler-Demyer syndrome
+3 more
GConflicting classifications of pathogenicity
FGFR1
(H528P +7 more)
Single nucleotide variant
(missense variant)
Hypogonadotropic hypogonadism 2 with or without anosmia
GUncertain significance
FGFR1
(Q398* +7 more)
Single nucleotide variant
(nonsense)
Hypogonadotropic hypogonadism 2 with or without anosmia
GLikely pathogenic
FGFR1
(R111S +5 more)
Single nucleotide variant
(missense variant)
Hypogonadotropic hypogonadism 2 with or without anosmia
GUncertain significance
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