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Items: 5

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
LYST
(Y3163C)
Single nucleotide variant
(missense variant)
Chédiak-Higashi syndrome
+1 more
GUncertain significance
TTC7A
(R325Q +1 more)
Single nucleotide variant
(missense variant +1 more)
not provided
+3 more
GConflicting classifications of pathogenicity
IKZF1
(M31V)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
ATM
Single nucleotide variant
(splice donor variant)
Familial cancer of breast
+2 more
GPathogenic/Likely pathogenic
ATM
Single nucleotide variant
(intron variant)
not provided
+3 more
GConflicting classifications of pathogenicity
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