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Items: 5

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
CHD1
(L1462Q +1 more)
Single nucleotide variant
(missense variant +1 more)
Pilarowski-Bjornsson syndrome
GUncertain significance
CHD1
(V1172L)
Single nucleotide variant
(missense variant +1 more)
Pilarowski-Bjornsson syndrome
GUncertain significance
CHD1
(D219V)
Single nucleotide variant
(missense variant +1 more)
Pilarowski-Bjornsson syndrome
GUncertain significance
CHD1
(D176G)
Single nucleotide variant
(missense variant +1 more)
Pilarowski-Bjornsson syndrome
GUncertain significance
CHD1
(S164fs)
Deletion
(frameshift variant +1 more)
Pilarowski-Bjornsson syndrome
GLikely pathogenic
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