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Items: 4

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
TTC7A
(F30fs +1 more)
Deletion
(frameshift variant +1 more)
Gastrointestinal defects and immunodeficiency syndrome 1
+1 more
GPathogenic/Likely pathogenic
TTC7A
(R112W +1 more)
Single nucleotide variant
(missense variant +1 more)
Gastrointestinal defects and immunodeficiency syndrome 1
+1 more
GUncertain significance
TTC7A
(R325Q +1 more)
Single nucleotide variant
(missense variant +1 more)
not provided
+3 more
GConflicting classifications of pathogenicity
TTC7A
(S505L +2 more)
Single nucleotide variant
(missense variant)
not provided
+2 more
GUncertain significance
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