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Items: 9

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
FOXI1
(Q148E)
Single nucleotide variant
(missense variant)
not provided
+1 more
GConflicting classifications of pathogenicity
FOXI1
(T226I)
Single nucleotide variant
(missense variant +1 more)
FOXI1-related condition
+3 more
GConflicting classifications of pathogenicity
FOXI1
Single nucleotide variant
(synonymous variant +1 more)
FOXI1-related condition
+3 more
GConflicting classifications of pathogenicity
FOXI1
(G258E)
Single nucleotide variant
(missense variant +1 more)
Pendred syndrome
+2 more
GUncertain significance
FOXI1
Single nucleotide variant
(synonymous variant +1 more)
not provided
+1 more
GConflicting classifications of pathogenicity
FOXI1
(G291R +1 more)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
FOXI1
(T301I +1 more)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
FOXI1
(G333S +1 more)
Single nucleotide variant
(missense variant)
Autosomal recessive nonsyndromic hearing loss 4
+1 more
GUncertain significance
FOXI1
(P340A +1 more)
Single nucleotide variant
(missense variant)
FOXI1-related condition
+3 more
GConflicting classifications of pathogenicity
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