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Items: 5

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
CCDC22
(A37V)
Single nucleotide variant
(missense variant)
Ritscher-Schinzel syndrome 2
GUncertain significance
CCDC22
(R64G)
Single nucleotide variant
(missense variant)
Ritscher-Schinzel syndrome 2
GUncertain significance
CCDC22
(R128Q)
Single nucleotide variant
(missense variant)
Ritscher-Schinzel syndrome 2
GUncertain significance
CCDC22
(R448L)
Single nucleotide variant
(missense variant)
Ritscher-Schinzel syndrome 2
GUncertain significance
CCDC22
(A537V)
Single nucleotide variant
(missense variant)
Ritscher-Schinzel syndrome 2
GUncertain significance
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